Process for preparing analgesic compounds

ABSTRACT

A process for preparing a compound of the formula (I): ##STR1## in which, R 1  and R 2  each represents hydrogen or C 1  -C 6  alkyl, or R 1  and R 2  together with the nitrogen atom to which they are attached form a heterocycle; E represents methylene, sulfur, oxygen or imino group optionally substituted with C 1  -C 6  alkyl or aralkyl; ring A is aryl or heteroaryl ring, optionally substituted; R 3  is hydrogen or C 1  -C 6  alkyl and R 4  is hydrogen or R 3  and R 4  together represent a group of formula (IV): 
     
         --(CR.sup.a R.sup.a).sub.m --C(═Y)--                   (IV) 
    
     (wherein R a  and R a  is C 1  -C 6  alkyl or hydrogen, up to a maximum of 3 alkyl groups, m is 1, 2, or 3, and Y is two hydrogens or oxygen); provided that when E represents a methylene group, then R 3  is a C 1  -C 6  alkyl group or R 3  and R 4  together represent a group of the formula (IV), which comprises reacting an acid of the formula ##STR2## with an amine of the formula ##STR3##

This application is a division of application Ser. No. 08/373,469 filed Jan. 17, 1995, (now U.S. Pat. No. 5,512,567) which is a continuation of application Ser. No. 08/140,602 filed Oct. 21, 1993 (abandoned), which is a division of application Ser. No. 07/943,386 filed Sep. 10, 1992 (now U.S. Pat. No. 5,270,327), which is a continuation of application Ser. No. 07/627,736 filed Dec. 14, 1990 (abandoned), which is a division of application Ser. No. 07/397,105 filed Aug. 22, 1989 (now U.S. Pat. No. 5,021,413).

BACKGROUND OF THE INVENTION

The present invention relates to carboxylic acid amide derivatives and pharmaceutically acceptable acid addition salts thereof, being compounds which have useful analgesic and other pharmaceutical activity, and further relates to the preparation of such compounds.

In general, analgesic drugs acting on κ-receptors do not show the side effects such as dependence, drug tolerance and respiratory inhibition shown by the morphine-like analgesic drugs acting on μ-receptors. Furthermore, analgesic drugs acting on κ-receptors do not show cross resistance to morphine. Accordingly, the analgesic drugs acting on κ-receptors are of considerable interest, because an agent which does not evince respiratory inhibition is useful for management of post-operative patients suffering from pain. Moreover, an agent without cross resistance is significant in clinical uses, for example, for patients suffering from cancer pain where tolerance to morphine and other antagonistic analgesic agents has occurred.

By way of example, European Patent Specification 232612 published on 19 Aug. 1987 discloses azacyclic compounds which exhibit κ-receptor agonism. The compounds are without the behavioural effects of morphine and morphine analogs, and are thus of potential therapeutic utility as analgesics. A small class of compounds within the generality of European Patent Specification 232612 and said to have improved properties are disclosed in European Patent Specification 260041 published on 16 Mar. 1988.

OBJECTS OF THE PRESENT INVENTION

The objects of the present invention include compounds which have pharmacological activity and in particular are useful as analgesic agents. Further objects comprise pharmaceutical compositions with analgesic or other pharmacological activity, as well as methods for the relief of pain using the compounds and processes for the preparation of such compounds.

SUMMARY OF THE PRESENT INVENTION

The present invention provides compounds of the general formula (I): ##STR4## in which,

R¹ and R² are the same or different and each represents a hydrogen atom or a C₁ -C₆ alkyl group, or R¹ and R² together with the nitrogen atom to which they are attached form a heterocyclic ring;

E represents a methylene group, a sulfur atom, an oxygen atom or an imino group optionally substituted with a C₁ -C₆ alkyl group or an aralkyl group;

the ring A represents an aryl ring; a heteroaryl ring; an aryl ring substituted with at least one substituent selected from Group (i); or a heteroaryl ring substituted with at least one substituent selected from Group (i);

said Group (i) comprising halogen atoms, C₁ -C₆ alkyl groups, halogenated C₁ -C₆ alkyl groups, C₁ -C₆ alkoxy groups, halogenated C₁ -C₆ alkoxy groups, C₁ -C₆ alkylthio groups, aryl groups, acyl groups, nitro groups, and hydroxy groups;

R³ represents a hydrogen atom or a C₁ -C₆ alkyl group and R⁴ represents a hydrogen atom, or R³ and R⁴ together represent a group of formula (IV):

    --(CR.sup.a R.sup.b).sub.m --C(═Y)--                   (IV)

(wherein each R^(a) and R^(b) represents hydrogen or a C₁ -C₃ alkyl group, provided that there are not more than three alkyl groups in the group of formula (IV), m represents 1, 2, or 3, and Y represents two hydrogen atoms or an oxygen atom);

provided that when E represents a methylene group, then R³ is a C₁ -C₆ alkyl group or R³ and R⁴ together represent a group of the formula (IV);

and pharmaceutically acceptable salts thereof.

Compounds wherein E represents a methylene group, and R³ and R⁴ both represent hydrogen atoms are excluded in view of the disclosure in European Patent Specification 232612, mentioned above.

The present invention thus embraces compounds of general formula (I) and salts thereof, wherein R³ is a C₁ -C₆ alkyl group and R⁴ is a hydrogen atom, or R³ and R⁴ together represent said group of formula (IV); and further embraces compounds of formula (I) wherein E is selected from the group consisting of a sulfur atom, an oxygen atom, an imino group, and imino groups substituted with a substituent selected from the group consisting of C₁ -C₆ alkyl groups and aralkyl groups; and R³ and R⁴ both represent hydrogen atoms.

PREFERRED EMBODIMENTS OF THE PRESENT INVENTION

Preferred embodiments include those compounds wherein R¹ and R² are the same or different and each is a C₁ -C₆ alkyl group, or R¹ and R² together with the nitrogen atom to which they are attached form a 5- or 6-membered heterocyclic ring;

E is selected from the group consisting of a methylene group, a sulfur atom and an imino group;

ring A is selected from the group consisting of aryl rings; heteroaryl rings; aryl rings substituted with at least one substituent of Group (ii); and heteroaryl rings substituted with at least one substituent of Group (ii);

said Group (ii) being a subset of Group (i) and comprising halogen atoms, halogenated C₁ -C₆ alkyl groups, and C₁ -C₆ alkyl groups;

R³ and R⁴ both represent hydrogen atoms, or R³ and R⁴ together represent a group of formula (IV):

    --(CR.sup.a R.sup.b).sub.m --C(═Y)--                   (IV)

(wherein each R^(a) and R^(b) represents hydrogen or a C₁ -C₃ alkyl group, provided that there is not more than one alkyl group in the group of formula (IV), m represents 1, or 2, and Y represents two hydrogen atoms or an oxygen atom);

and pharmaceutically acceptable salts thereof.

More preferred embodiments include those compounds wherein R¹ and R² are the same or different and each is a C₁ -C₃ alkyl group, or R¹ and R² together with the nitrogen atom to which they are attached form a pyrrolidine ring or a piperidine ring;

E is selected from the group consisting of a methylene group and a sulfur atom;

ring A is selected from the group consisting of aryl rings; heteroaryl rings; and aryl rings substituted with at least one substituent selected from the group consisting of halogen atoms, halogenated C₁ -C₃ alkyl groups, and C₁ -C₃ alkyl groups;

R³ and R⁴ both represent hydrogen atoms, or R³ and R⁴ together represent a group of formula (IV):

    --(CR.sup.a R.sup.b).sub.m --C(═Y)--                   (IV)

(wherein each R^(a) and R^(b) represents a hydrogen atom; m represents 1, or 2, and Y represents two hydrogen atoms or an oxygen atom);

and pharmaceutically acceptable salts thereof.

Most preferred embodiments include those compounds wherein R¹ and R² together with the nitrogen atom to which they are attached form a pyrrolidine ring or a piperidine ring;

E is selected from the group consisting of a methylene group and a sulfur atom;

ring A is selected from the group consisting of aryl rings and aryl rings substituted with at least one substituent selected from the group consisting of halogen atoms and C₁ -C₃ alkyl groups;

R³ and R⁴ together represent a group of formula (IV):

    --(CR.sup.a R.sup.b).sub.m --C(═Y)--                   (IV)

(wherein each R^(a) and R^(b) represents hydrogen atom, m represents 1, or 2, and Y represents two hydrogen atoms or an oxygen atom);

and pharmaceutically acceptable salts thereof.

Further embodiments include:

compounds wherein R¹ and R² together with the nitrogen atom to which they are attached form a pyrrolidine ring or a piperidine ring;

E is selected from the group consisting of a methylene group and a sulfur atom;

ring A is an aryl ring substituted with at least one substituent selected from the group consisting of halogen atoms and C₁ -C₃ alkyl groups;

R³ and R⁴ together represent a group of formula (IV):

    --(CR.sup.a R.sup.b).sub.m --C(═Y)--                   (IV)

(wherein each R^(a) and R^(b) represents a hydrogen atom, m represents 1 or 2, and Y represents two hydrogen atoms or an oxygen atom);

compounds wherein R¹ and R² both represent C₁ -C₃ alkyl groups;

E is selected from the group consisting of a methylene group and a sulfur atom;

ring A is selected from the group consisting of aryl rings; aryl rings substituted with at least one substituent selected from the group comprising halogen atoms and C₁ -C₃ alkyl groups;

R³ and R⁴ together represent a group of formula (IV):

    --(CR.sup.a R.sup.b).sub.m --C(═Y)--                   (IV)

(wherein each R^(a) and R^(b) represents a hydrogen atom, m represents 1 or 2, and Y represents two hydrogen atoms or an oxygen atom);

compounds wherein R¹ and R² both represent C₁ -C₃ alkyl groups;

E is selected from the group consisting of a methylene group and a sulfur atom;

ring A is an aryl ring substituted with at least one substituent selected from the group consisting of halogen atoms and C₁ -C₃ alkyl groups;

R³ and R⁴ together represent a group of formula (IV):

    --(CR.sup.a R.sup.b).sub.m --C(═Y)--                   (IV)

(wherein each R^(a) and R^(b) represents a hydrogen atom, m represents 1 or 2, and Y represents two hydrogen atoms or an oxygen atom);

compounds wherein R¹ and R² together with the nitrogen atom to which they are attached form a pyrrolidine ring or a piperidine ring;

compounds wherein E is selected from the group consisting of a methylene group and a sulfur atom;

compounds wherein ring A is selected from the group consisting of aryl rings and aryl rings substituted with at least one substituent selected from the group consisting of halogen atoms and C₁ -C₃ alkyl groups; and

compounds wherein R³ and R⁴ together represent a group of formula (IV):

    --(CR.sup.a R.sup.b).sub.m --C(═Y)--                   (IV)

(wherein each R^(a) and R^(b) represents a hydrogen atom, m represents 1, or 2, and Y represents two hydrogen atoms or an oxygen atom);

and pharmaceutically acceptable salts thereof.

In the general formula (I), the groups R¹ and R² are the same or different and each represents a hydrogen atom, or a straight or branched chain C₁ -C₆ alkyl group preferably having from 1 to 3 carbon atoms. Examples of suitable alkyl groups include a methyl, ethyl, propyl, isopropyl, butyl, isobutyl, s-butyl, t-butyl, pentyl, isopentyl, 2-methylbutyl, t-pentyl, neopentyl, hexyl, 4-methylpentyl, 3-methylpentyl, 2-methylpentyl, 3,3-dimethylbutyl-2,2-dimethylbutyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 2,3-dimethylbutyl, or 1,3-dimethylbutyl group. Of these, a methyl, ethyl, propyl, or isopropyl group is preferred.

Alternatively, R¹ and R² together with the nitrogen atom to which they are attached form a heterocyclic ring, preferably a saturated heterocyclic ring, and more preferably a 5- or 6-membered N-heterocycle optionally having a further heteroatom which may be oxygen, nitrogen or sulfur. Examples of suitable heterocyclic radicals represented by such rings include an imidazolidinyl, hexahydropyridazinyl, hexahydropyrimidinyl, piperazinyl, hexamethyleneimino, 1,2-diazacycloheptyl, 1,3-diazacycloheptyl, homopiperazinyl, pyrrolyl, azepinyl, thiazolidinyl, morpholinyl, thiomorpholinyl, pyrazolyl, imidazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, 1,2,3-oxadiazolyl, triazolyl, tetrazolyl, thiadiazolyl, pyridyl, pyridazinyl, pyrimidinyl, pyrazinyl, quinolyl, isoquinolyl, acridyl, tetrahydroacridyl, pyrrolidinyl, piperidino, tetrahydroquinolyl, tetrahydroisoquinolyl, isoindolyl, indolinyl or 6-azabicyclo[3.2.1]oct-6-yl group. The heterocyclic ring may be substituted with a straight or branched chain C₁ -C₆ alkyl group, preferably an alkyl group having 1 to 3 carbon atoms. For example, a 6-azabicyclo[3.2.1]oct-6-yl ring may be 1,3,3-trimethyl substituted, and a piperazine ring may be N-substituted for instance with a straight or branched chain C₁ -C₆ alkyl group, preferably an alkyl group having 1 to 3 carbon atoms, such as a methyl, ethyl, propyl or isopropyl group. Preferred heterocyclic rings which may be formed by R¹ and R² comprise a pyrrolidine, piperidine, N-methylpiperazine, morpholine, hexamethyleneimino or thiazolidine ring.

Particularly preferred examples for the group formed by R¹ and R² together with the nitrogen to which they are attached include monoalkyl- and dialkyl-substituted amino groups in which the or each alkyl group contains from 1 to 6, preferably from 1 to 3, carbon atoms such as a methylamino, ethylamino, propylamino, isopropylamino, butylamino, isobutylamino, dimethylamino, diethylamino, dipropylamino, diisopropylamino, pentylamino or hexylamino group, of which a methylamino, dimethylamino, ethylamino, propylamino, or isopropylamino group is preferred. The particularly preferred examples for the group formed by R¹ and R² together with the nitrogen to which they are attached further include a heterocyclic radical such as a 1-pyrrolidinyl, 1-piperidyl (that is, piperidino), 1-(4-methylypiperazinyl, 1-hexamethyleneiminyl, 3-thiazolidinyl, or 4-morpholinyl (that is, morpholino) group.

The symbol E represents a methylene group, a sulfur atom, an oxygen atom or an imino group. The imino group can be substituted with a C₁ -C₆ alkyl group or with an aralkyl group having 1 to 4 carbon atoms in the alkyl part and 6 or 10 carbon atoms in the aryl part. Examples of such substitutent groups for an imino group include a benzyl, phenethyl, 1-phenylethyl, 1-phenylpropyl, 2-phenylpropyl, 3-phenylpropyl, 4-phenylbutyl, 1-naphthylmethyl or 2-naphthylmethyl groups more preferably a C₇ -C₉ aralkyl group such as a benzyl group.

The ring A is preferably an aromatic ring such as an aryl ring, for instance a benzene or naphthalene ring, or a 5- to 7-membered heteroaryl ring containing 1 to 3 oxygen heteroatoms, nitrogen heteroatoms and/or sulfur heteroatoms, optionally condensed with a further ring. Heteroaryl examples for the ring A include a furan, thiophene, pyrazole, imidazole, oxazole, isoxazole, thiazole, isothiazole, triazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, quinoline, isoquinoline, or acridine ring. Preferably the ring A is a benzene ring or a 5- or 6-membered heteroaryl ring containing 1 heteroatom, such as a thiophene, furan or pyridine ring.

The ring A may be substituted by one or more substituents, preferably 1 to 3 substituents, and typically 1 or 2 substituents, the substituents being of the Group (i). Such substituents may be halogen atoms such as a fluorine, chlorine, bromine and/or iodine atom; straight or branched chain C₁ -C₆ alkyl groups, typically those mentioned for R¹ or R², and preferably straight or branched chain alkyl groups having 1 to 3 carbon atoms such as a methyl, ethyl, n-propyl or isopropyl group; aryl groups, preferably a C₆ or C₁₀ aryl group, that is a phenyl or naphthyl group; acyl groups, typically carboxylic acyl groups, preferably aliphatic acyl groups containing from 1 to 6, more preferably 1 to 4, carbon atoms such as a formyl, acetyl, propionyl, butyryl, isobutyryl, valeryl, isovaleryl, pivaloyl or hexanoyl group, of which a formyl, acetyl, propionyl, butyryl or isobutyryl group is especially preferred; straight or branched chain C₁ -C₆ alkoxy groups, preferably having 1 to 3 carbon atoms, such as a methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, pentyloxy, isopentyloxy, t-pentyloxy or hexyloxy group; nitro groups; halogenated C₁ -C₆ alkyl or alkoxy groups, preferably C₁ -C₃ alkyl or alkoxy groups such as a fluoromethyl, difluoromethyl, trifluoromethyl, 1-fluoroethyl, 2-fluoroethyl,

2,2-difluoroethyl, 2,2,2-trifluoroethyl, 3-fluoropropyl,

4-fluorobutyl, 5-fluoropentyl, 6-fluorohexyl,

3,3-difluoropropyl, 3,3,3-trifluoropropyl,

4,4-difluorobutyl, 4,4,4-trifluorobutyl, bromomethyl,

dibromomethyl, trichloromethyl, 1-chloroethyl,

2-bromoethyl, 2,2-dibromoethyl, 2,2,2-trichloroethyl,

fluoromethoxy, difluoromethoxy, trifluoromethoxy,

1-fluoroethoxy, 2-fluoroethoxy, 2,2-difluoroethoxy,

2,2,2-trifluoroethoxy, 3-fluoropropoxy, 4-fluorobutoxy,

5-fluoropentyloxy, 6-fluorohexyloxy,

3,3-difluoropropoxy, 3,3,3-trifluoropropoxy,

4,4-difluorobutoxy or 4,4,4-trifluorobutoxy group, of which a fluoromethyl, difluoromethyl, trifluoromethyl, 1-fluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl or 2,2,2-trifluoroethyl group is especially preferred; hydroxy groups; or straight or branched chain C₁ -C₆ alkylthio groups, preferably straight or branched chain alkylthio groups having 1 to 3 carbon atoms, such as a methylthio, ethylthio, n-propylthio, isopropylthio, butylthio, isobutylthio, s-butylthio, t-butylthio, pentylthio, isopentylthio, 2-methylbutylthio,

t-pentylthio, neo-pentylthio, hexylthio,

4-methylpentylthio, 3-methylpentylthio,

2-methylpentylthio, 3,3-dimethylbutylthio,

2,2-dimethylbutylthio, 1,1-dimethylbutylthio,

1,2-dimethylbutylthio, 2,3-dimethylbutylthio, or

1,3-dimethylbutylthio group.

Typical examples for the ring A include an aryl ring which is not substituted, such as, for example, a benzene or naphthalene ring; an aryl ring which is substituted with an alkyl group such as, for example, a

4-methylbenzene, 2-methylbenzene, 3-methylbenzene,

4-ethylbenzene, 4-butylbenzene, 2-propylbenzene,

3-hexylbenzene, 2,3-dimethylbenzene,

3,4-dimethylbenzene, 2,5-dimethylbenzene,

2,6-dimethylbenzene, 2,4-dimethylbenzene,

2,3-diethylbenzene, 3,4-dipropylbenzene,

2,5-dibutylbenzene, 2,6-dipentylbenzene,

2,4-dihexylbenzene, 2,3,6-trimethylbenzene,

2,3,4-trimethylbenzene, 3,4,5-trimethylbenzene,

2,5,6-trimethylbenzene, 2,4,6-trimethylbenzene,

2,3,6-triethylbenzene, 2,3,4-tripropylbenzene,

3,4,5-tributylbenzene, 2,5,6-tripentylbenzene,

2,4,6-trihexylbenzene, 1-methyl-2-naphthalene,

2-methyl-1-naphthalene, 3-methyl-1-naphthalene,

2-ethyl-1-naphthalene, 1-butyl-2-naphthalene,

2-propyl-1-naphthalene, 3-hexyl-1-naphthalene,

2,3-dimethyl-1-naphthalene, 3,8-dimethyl-1-naphthalene,

4,8-dimethyl-1-naphthalene, 5,6-dimethyl-1-naphthalene,

2,4-dimethyl-1-naphthalene, 2,3-diethyl-1-naphthalene,

3,4-dipropyl-1-naphthalene, 4,5-dibutyl-1-naphthalene,

5,6-dipentyl-1-naphthalene, 2,4-dihexyl-1-naphthalene,

2,3,6-trimethyl-1-naphthalene,

2,3,4-trimethyl-1-naphthalene,

3,4,5-trimethyl-1-naphthalene,

4,5,6-trimethyl-1-naphthalene,

2,4,8-trimethyl-1-naphthalene,

2,3,6-triethyl-1-naphthalene,

2,3,4-tripropyl-1-naphthalene,

3,4,8-tributyl-1-naphthalene,

4,5,6-tripentyl-1-naphthalene or

2,4,6-trihexyl-1-naphthalene ring; an aryl ring which is substituted with a halogen atom such as, for example, a

4-fluorobenzene, 2-fluorobenzene, 3-fluorobenzene,

4-bromobenzene, 2-iodobenzene, 3-chlorobenzene,

4-chlorobenzene, 3,5-difluorobenzene,

2,5-difluorobenzene, 2,5-diiodobenzene,

2,6-difluorobenzene, 2,4-difluorobenzene,

2,3-dichlorobenzene, 3,4-dichlorobenzene,

2,5-dichlorobenzene, 2,6-dichlorobenzene,

2,4-dibromobenzene, 2,3,6-trifluorobenzene,

2,3,4-trifluorobenzene, 3,4,5-trifluorobenzene,

2,5,6-trifluorobenzene, 2,4,6-trifluorobenzene,

2,3,6-trichlorobenzene, 2,3,4-trichlorobenzene,

3,4,5-tribromobenzene, 2,5,6-tribromobenzene,

2,4,6-tribromobenzene, 1-fluoro-2-naphthalene,

2-fluoro-1-naphthalene, 3-fluoro-1-naphthalene,

2-chloro-1-naphthalene, 1-chloro-2-naphthalene,

2-bromo-1-naphthalene, 3-bromo-1-naphthalene,

2,3-difluoro-1-naphthalene, 3,8-difluoro-1-naphthalene,

4,8-difluoro-1-naphthalene, 5,6-difluoro-1-naphthalene,

2,4-difluoro-1-naphthalene, 2,3-dichloro-1-naphthalene,

3,4-dichloro-1-naphthalene, 4,5-dichloro-1-naphthalene,

5,6-dibromo-1-naphthalene, 2,4-dibromo-1-naphthalene,

2,3,6-trifluoro-1-naphthalene,

2,3,4-trifluoro-1-naphthalene,

3,4,5-trifluoro-1-naphthalene,

4,5,6-trifluoro-1-naphthalene,

2,4,8-trifluoro-1-naphthalene,

2,3,6-trichloro-1-naphthalene,

2,3,4-trichloro-1-naphthalene

3,4,8-tribromo-1-naphthalene,

4,5,6-tribromo-1-naphthalene or

2,4,6-tribromo-1-naphthalene ring; an aryl ring which is substituted with a lower alkoxy group such as, for example, a 4-methoxybenzene, 2-methoxybenzene,

3-methoxybenzene, 4-ethoxybenzene, 4-propoxybenzene,

2-butoxybenzene, 3-ethoxybenzene, 3,5-dimethoxybenzene,

2,5-dimethoxybenzene, 2,5-dipropoxybenzene,

2,6-dimethoxybenzene, 2,4-dimethoxybenzene,

2,3-diethoxybenzene, 3,4-diethoxybenzene,

2,5-diethoxybenzene, 2,6-diethoxybenzene,

2,4-dipropoxybenzene, 2,3,6-trimethoxybenzene,

2,3,4-trimethoxybenzene, 3,4,5-trimethoxybenzene,

2,5,6-methoxybenzene, 2,4,6-trimethoxybenzene,

2,3,6-triethoxybenzene, 2,3,4-triethoxybenzene,

3,4,5-tripropoxybenzene, 2,5,6-tripropoxybenzene,

2,4,6-tripropoxybenzene, 1-methoxy-2-naphthalene,

2-methoxy-1-naphthalene, 3-methoxy-1-naphthalene,

2-ethoxy-1-naphthalene, 1-ethoxy-2-naphthalene,

2-propoxy-1-naphthalene, 3-propoxy-1-naphthalene,

2,3-dimethoxy-1-naphthalene,

3,8-dimethoxy-1-naphthalene,

4,8-dimethoxy-1-naphthalene,

5,6-dimethoxy-1-naphthalene,

2,4-dimethoxy-1-naphthalene,

2,3-dimethoxy-1-naphthalene, 3,4-diethoxy-1-naphthalene,

4,5-diethoxy-1-naphthalene, 5,6-dipropoxy-1-naphthalene,

2,4-dipropoxy-1-naphthalene,

2,3,6-trimethoxy-1-naphthalene,

2,3,4-trimethoxy-1-naphthalene,

3,4,5-trimethoxy-1-naphthalene,

4,5,6-trimethoxy-1-naphthalene,

2,4,8-trimethoxy-1-naphthalene,

2,3,6-triethoxy-1-naphthalene,

2,3,4-triethoxy-1-naphthalene,

3,4,8-tripropoxy-1-naphthalene,

4,5,6-tripropoxy-1-naphthalene or

2,4,6-tripropoxy-1-naphthalene ring; an heteroaryl ring which is unsubstituted, such as, for example, a thiophene or furan ring; an heteroaryl ring which is substituted with an alkyl group such as, for example, a

4-methylthiophene, 2-methylthiophene, 3-methylthiophene,

4-ethylthiophene, 4-butylthiophene, 2-propylthiophene,

3-hexylthiophene, 2,3-dimethylthiophene,

3,4-dimethylthiophene, 2,5-dimethylthiophene,

2,4-dimethylthiophene, 2,3-diethylthiophene,

3,4-dipropylthiophene, 2,5-dibutylthiophene,

2,4-dihexylthiophene, 2,3,4-trimethylthiophene,

3,4,5-trimethylthiophene, 2,3,4-tripropylthiophene,

3,4,5-tributylthiophene; an heteroaryl zing which is substituted with a halogen atom such as, for example, a

4-fluorothiophene, 2-fluorothiophene, 3-fluorothiophene,

4-bromothiophene, 2-iodothiophene, 3-chlorothiophene,

3,5-difluorothiophene, 2,5-difluorothiophene,

2,5-diiodothiophene, 2,4-difluorothiophene,

2,3-dichlorothiophene, 3,4-dichlorothiophene,

2,5-dichlorothiophene, 2,4-dibromothiophene,

2,3,4-trifluorothiophene, 3,4,5-trifluorothiophene,

2,3,4-trichlorothiophene, or 3,4,5-tribromothiophene ring; an heteroaryl zing which is substituted with a lower alkoxy group such as, for example, a

4-methoxythiophene, 2-methoxythiophene,

3-methoxythiophene, 4-ethoxythiophene,

4-propoxythiophene, 2-butoxythiophene,

3-ethoxythiophene, 3,5-dimethoxythiophene,

2,5-dimethoxythiophene, 2,5-dipropoxythiophene,

2,4-dimethoxythiophene, 2,3-diethoxythiophene,

3,4-diethoxythiophene, 2,5-diethoxythiophene,

2,4-dipropoxythiophene, 2,3,4-trimethoxythiophene,

3,4,5-trimethoxythiophene, 2,3,4-triethoxythiophene, or

3,4,5-tripropoxythiophene ring; an aryl ring which is substituted with an alkylthio group such as, for example, a 4-methylthiobenzene, 2-methylthiobenzene,

3-methylthiobenzene, 4-ethylthiobenzene,

4-butylthiobenzene, 2-propylthiobenzene, or

3-hexylthiobenzene ring; an heteroaryl zing which is substituted with an alkylthio group such as, for example, a 4-methylthiothiophene, 2-methylthiothiophene,

3-methylthiothiophene, 4-ethylthiothiophene, or

4-butylthiothiophene ring; an aryl ring which is substituted with a hydroxy group such as, for example, a

4-hydroxybenzene, 2-hydroxybenzene, or 3-hydroxybenzene ring; an heteroaryl ring which is substituted with a hydroxy group such as, for example, a

4-hydroxythiophene, 2-hydroxythiophene,

3-hydroxythiophene ring; an aryl ring which is substituted with a nitro group such as, for example, a

4-nitrobenzene, 2-nitrobenzene, or 3-nitrobenzene ring; or an heteroaryl ring which is substituted with a nitro group such as, for example, a 4-nitrothiophene,

2-nitrothiophene, 3-nitrothiophene ring.

Preferred examples for the ring A include an aryl or, heteroaryl ring which is not substituted, or a benzene or thiophene ring substituted by one or more halogen atoms such as a fluorine or chlorine atom; by one or more C₁ -C₃ alkyl groups such as a methyl or ethyl group; by a C₁ -C₃ alkoxy group such as a methoxy or ethoxy; by a hydroxy group; by a nitro group; or by a C₁ -C.sub. 3 alkylthio group such as a methylthio group.

R³ is a hydrogen atom or a C₁ -C₆ alkyl group and R⁴ is a hydrogen atom. In this case, it is preferred that R³ is a hydrogen atom or a C₁ -C₃ alkyl group and R⁴ is a hydrogen atom, and more preferred that both R³ and R⁴ represent hydrogen atoms. R.sup. 3 and R⁴ can alternatively together represent a group of formula (IV):

    --(CR.sup.a R.sup.b).sub.m --C(═Y)--                   (IV)

(wherein each R^(a) and R^(b) represents hydrogen or a C₁ -C₃ alkyl group, provided that there are not more than three alkyl groups in the group of formula (IV), m represents 1, 2, or 3, and Y represents two hydrogen atoms or an oxygen atom). In this case, the compounds of formula (I) are then of the general formula (Ia): ##STR5## In the formulae (Ia) and (IV), both R^(a) and R^(b) preferably represent hydrogen atoms, and m is preferably 1 or 2.

The present invention further embraces pharmaceutically acceptable non-toxic salts of the compounds of general formula (I). Examples of suitable salts include acid addition salts with an inorganic acid for instance a hydrohalogenated acid such as hydrofluoric acid, hydrochloric acid, hydrobromic acid or hydroiodic acid, or nitric acid, perchloric acid, sulfuric acid, phosphoric acid or the like acid; and acid addition salts with an an organic acid for instance a lower alkyl sulfonic acid such as methanesulfonic acid, trifluoromethanesulfonic acid or ethanesulfonic acid, an aryl sulfonic acid such as benzenesulfonic acid or p-toluenesulfonic acid, an amino acid such as glutamic acid or aspargic acid, or an organic carboxylic acid such as fumaric acid, succinic, acid, citric acid, tartaric acid, oxalic acid, mandelic acid, maleic acid or the like acid.

The compounds of general formula (I) exist in more than one stereoisomeric form, and this invention embraces individual isomers as well as mixtures. It will often be the case that one stereoisomer is more active than another, as may be determined by routine testing.

Preferred isomers of this invention include those compounds and salts wherein

the group E is a methylene group and the configuration at the carbon having the substituent --CH₂ NR¹ R² is the (S) configuration;

the group E is a sulphur atom and the configuration at the carbon having the substituent --CH₂ NR¹ R² is the (R) configuration;

the group E is an oxygen atom and the configuration at the carbon having the substituent --CH₂ NR¹ R² is the (R) configuration; or

the group E is an optionally substituted imino group and the configuration at the carbon having the substituent --CH₂ NR¹ R² has the chirality corresponding to the (R) configuration for the case where E is an imino group and the substituent is --CH₂ NH₂. In this last respect, the nomenclature for the configuration at the carbon having the substituent --CH₂ NR¹ R² for compounds with the preferred chirality will be (R) or (S), depending on the nature of the imino substituent, the group R¹ and the group R².

Furthermore, the compounds of this invention may exist as solvates, particularly hydrates, and this invention extends to such solvates.

Compounds of the general formula (I) in accordance with the present invention are exemplified by the following compounds, by their salts, especially the hydrochloride or methanesulfonate salts, and by their individual diastereoisomers and their individual optical isomers.

1. 1-(indan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine

2. 1-(3-oxoindan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine

3. 1-(5-chloro-3-oxoindan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine

4. 1-(5-methyl-3-oxoindan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine

5. 1-(5-nitro-3-oxoindan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine

6. 1-(5-methoxy-3-oxoindan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine

7. 1-(6-chloro-3-oxoindan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine

8. 1-(6-methoxy-3-oxoindan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine

9. 1-(5,6-dichloro-3-oxoindan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine

10. 1-(4,5-dichloro-3-oxoindan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine

11. 1-(6-hydroxy-3-oxoindan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine

12. 4-(5-methyl-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1ylmethyl)morpholine

13. 4-(6,7-dichloro-1,2,3,4-tetrahydronaphthoyl)-3-(piperidinomethyl)thiomorpholine

14. 1-(5,6-dichloroindan-1-carbonyl)-2-(piperidinomethyl)piperidine

15. 1-(3-oxoindan-1-carbonyl)-2-(piperidinomethyl)piperidine

16. 1-(5,6-dichloro-3-oxoindan-1-carbonyl)-2-(piperidinomethyl)piperidine

17. 2-(pyrrolidin-1-ylmethyl)-1-(1,2,3,4-tetrahydro-4-oxo-1-naphthoyl)piperidine

18. 1-(6,7-dichloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl)-2-(pyrrolidin-1-ylmethyl)piperidine

19. 4,5-dihydro-6-oxo-4-[2-(pyrrolidin-1-ylmethyl)piperidine-1-carbonyl]-6H-cyclopenta[b]thiophene

20. 4,5-dihydro-6-oxo-4-[2-(pyrrolidin-1-ylmethyl)piperidine-1-carbonyl]-6H-cyclopenta[b]furan

21. 2-chloro-4,5-dihydro-6-oxo-4-[2-(pyrrolidin-1-ylmethyl)piperidine-1-carbonyl]-6H-cyclopenta[b]-thiophene

22. 1-(5,6-dichloro-3-oxoindan-1-carbonyl)-2-(4-methylpiperazin-1-ylmethyl)piperidine

23. 4-[2-(3,4-dichlorophenyl)propionyl]-3-(pyrrolidin-1-ylmethyl)thiomorpholine

24. 4-[2-(3,4-dichlorophenyl)propionyl]-3-(pyrrolidin-1-ylmethyl)morpholine

25. 4,5-dihydro-6-oxo-4-[3-(pyrrolidin-1-ylmethyl)thiomorpholine-4-carbonyl]-6H-cyclopenta[b]-thiophene

26. 4,5-dihydro-4-[3-(pyrrolidin-1-ylmethyl)thiomorpholine-4-carbonyl]-6H-cyclopenta[b]-thiophene

27. 4,5-dihydro-6-oxo-4-[3-(pyrrolidin-1-ylmethyl)thiomorpholine-4-carbonyl]-6H-cyclopenta[b]furan

28. 4,5,6,7-tetrahydro-7-oxo-4-[3-(pyrrolidin-1-ylmethyl)thiomorpholine-4-carbonyl]benzo[b]-thiophene

29. 4-(2,2-dimethyl-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

30. 4-(3,4-dichlorophenylacetyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

31. 4-(4-chlorophenylacetyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

32. 4-(4-methylphenylacetyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

33. 4-(4-methoxyphenylacetyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

34. 4-(4-methylthiophenylacetyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

35. 4-(4-nitrophenylacetyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

36. 4-(3,4-dichlorophenylacetyl)-3-(pyrrolidin-1-ylmethyl)morpholine

37. 4-(4-chlorophenylacetyl)-3-(pyrrolidin-1-ylmethyl)morpholine

38. 4-(4-methylphenylacetyl)-3-(pyrrolidin-1-ylmethyl)morpholine

39. 4-(4-methoxyphenylacetyl)-3-(pyrrolidin-1-ylmethyl)morpholine

40. 4-(4-methylthiophenylacetyl)-3-(pyrrolidin-1-ylmethyl)morpholine

41. 4-(4-nitrophenylacetyl)-3-(pyrrolidin-1-ylmethyl)morpholine

42. 1-(3,4-dichlorophenylacetyl)-4-methyl-2-(pyrrolidin-1-ylmethyl)piperazine

43. 1-(4-chlorophenylacetyl)-4-methyl-2-(pyrrolidin-1-ylmethyl)piperazine

44. 4-methyl-1-(4-methylphenylacetyl)-2-(pyrrolidin-1-ylmethyl)piperazine

45. 1-(4-methoxyphenylacetyl)-4-methyl-2-(pyrrolidin-1-ylmethyl)piperazine

46. 4-methyl-1-(4-methylthiophenylacetyl)-2-(pyrrolidin-1-ylmethyl)piperazine

47. 4-methyl-1-(4-nitrophenylacetyl)-2-(pyrrolidin-1-ylmethyl)piperazine

48. 4-(4-biphenylacetyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

49. 4-(3,4-dichlorophenylacetyl)-3-(piperidinomethyl)thiomorpholine

50. 4-(3,4-dichlorophenylacetyl)-3-(morpholinomethyl)thiomorpholine

51. 3-(pyrrolidin-1-ylmethyl)-4-(2-thienylacetyl)thiomorpholine

52. 4-(1-naphthylacetyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

53. 4-(3-pyridylacetyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

54. 4-(4-biphenylacetyl)-3-(pyrrolidin-1-ylmethyl)morpholine

55. 4-(3,4-dichlorophenylacetyl)-3-(piperidinomethyl)morpholine

56. 4-(3,4-dichlorophenylacetyl)-3-(morpholinomethyl)morpholine

57. 3-(pyrrolidin-1-ylmethyl)-4-(2-thienylacetyl)morpholine

58. 4-(1-naphthylacetyl)-3-(pyrrolidin-1-ylmethyl)morpholine

59. 4-(3-pyridylacetyl)-3-(pyrrolidin-1-ylmethyl)morpholine

60. 4-methyl-2-(pyrrolidin-1-ylmethyl)-1-(2-thienylacetyl)piperazine

61. 4-methyl-1-(1-naphthylacetyl)-2-(pyrrolidin-1-ylmethyl)piperazine

62. 4-methyl-1-(3-pyridylacetyl)-2-(pyrrolidin-1-ylmethyl)piperazine

63. 4-(3,4-dichlorophenylacetyl)-3-(dimethylaminomethyl)thiomorpholine

64. 4-(3,4-dichlorophenylacetyl)-3-(dimethylaminomethyl)morpholine

65. 4-(3,4-difluorophenylacetyl)-3-(pyrrolidin-1-ylmethyl)morpholine

66. 4-(3,4-dichlorophenylacetyl)-3-(4-methylpiperazin-1-ylmethyl)morpholine

67. 4-(indan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

68. 4-(3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

69. 4-(5-chloroindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

70. 4-(5-chloro-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

71. 4-(5-isopropylindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

72. 4-(5-methylindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

73. 4-(5-methyl-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

74. 4-(5-methoxyindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

75. 4-(5-methoxy-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

76. 4-(5-isopropyl-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

77. 4-(7-chloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

78. 4-(7-chloro-1,2,3,4-tetrahydro-1-naphthoyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

79. 4-(6,7-dichloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

80. 4-(6,7-dichloro-1,2,3,4-tetrahydro-1-naphthoyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

81. 4-(7-chloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl)-3-(morpholinomethyl)thiomorpholine

82. 4-(7-chloro-1,2,3,4-tetrahydro-1-naphthoyl)-3-(morpholinomethyl)thiomorpholine

83. 4-(6,7-dichloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl)-3-(morpholinomethyl)thiomorpholine

84. 4-(6,7-dichloro-1,2,3,4-tetrahydro-1-naphthoyl)-3-(morpholinomethyl)thiomorpholine

85. 4-(6,7-difluoro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

86. 4-(6,7-difluoro-1,2,3,4-tetrahydro-1-naphthoyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

87. 3-(pyrrolidin-1-ylmethyl)-4-(1,2,3,4-tetrahydro-7-methyl-4-oxo-1-naphthoyl)thiomorpholine

88. 3-(pyrrolidin-1-ylmethyl)-4-(1,2,3,4-tetrahydro-7-methyl-1-naphthoyl)thiomorpholine

89. 3-(pyrrolidin-1-ylmethyl)-4-(1,2,3,4-tetrahydro-7-isopropyl-4-oxo-1-naphthoyl)thiomorpholine

90. 3-(pyrrolidin-1-ylmethyl)-4-(1,2,3,4-tetrahydro-7-isopropyl-1-naphthoyl)thiomorpholine

91. 4-(1,2,3,4-tetrahydro-7-methyl-4-oxo-1-naphthoyl)-3-(morpholinomethyl)thiomorpholine

92. 3-(morpholinomethyl)-4-(1,2,3,4-tetrahydro-7-methyl-1-naphthoyl)thiomorpholine

93. 3-(morpholinomethyl)-4-(1,2,3,4-tetrahydro-4-oxo-1-naphthoyl)thiomorpholine

94. 3-(morpholinomethyl)-4-(1,2,3,4-tetrahydro-1-naphthoyl)thiomorpholine

95. 4-(5,6-dichloroindan-1-carbonyl)-3-(morpholinomethyl)thiomorpholine

96. 4-(5,6-dichloroindan-1-carbonyl)-3-(4-methylpiperazin-1-ylmethyl)thiomorpholine

97. 4-(5,6-dichloro-3-oxoindan-1-carbonyl)-3-(morpholinomethyl)thiomorpholine

98. 4-(5,6-dichloro-3-oxoindan-1-carbonyl)-3-(4-methylpiperazin-1-ylmethyl)thiomorpholine

99. 4-(indan-1-carbonyl)-3-(piperidinomethyl)thiomorpholine

100. 4-(3-oxoindan-1-carbonyl)-3-(piperidinomethyl)thiomorpholine

101. 4-(5-chloroindan-1-carbonyl)-3-(piperidinomethyl)thiomorpholine

102. 4-(5-chloro-3-oxoindan-1-carbonyl)-3-(piperidinomethyl)thiomorpholine

103. 4-(6-chloroindan-1-carbonyl)-3-(piperidinomethyl)thiomorpholine

104. 4-(5-methylindan-1-carbonyl)-3-(piperidinomethyl)thiomorpholine

105. 4-(5-methyl-3-oxoindan-1-carbonyl)-3-(piperidinomethyl)thiomorpholine

106. 4-(5-isopropylindan-1-carbonyl)-3-(piperidinomethyl)thiomorpholine

107. 4-(5-isopropyl-3-oxoindan-1-carbonyl)-3-(piperidinomethyl)thiomorpholine

108. 4-(6-chloro-3-oxoindan-1-carbonyl)-3-(piperidinomethyl)thiomorpholine

109. 4-(6-chloroindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

110. 4-(6-chloro-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

111. 4-(6-methylindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

112. 4-(6-methyl-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

113. 4-(5,6-dichloroindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

114. 4-(6-methoxyindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

115. 4-(6-methoxy-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

116. 4-(6-isopropylindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

117. 4-(6-isopropyl-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

118. 4-(5,6-dichloro-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

119. 3-(piperidinomethyl)-4-(1,2,3,4-tetrahydro-4-oxo-1-naphthoyl)thiomorpholine

120. 3-(piperidinomethyl)-4-(1,2,3,4-tetrahydro-1-naphthoyl)thiomorpholine

121. 4-(6-chloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl)-3-(piperidinomethyl)thiomorpholine

122. 4-(6-chloro-1,2,3,4-tetrahydro-1-naphthoyl)-3-(piperidinomethyl)thiomorpholine

123. 3-(piperidinomethyl)-4-(1,2,3,4-tetrahydro-6-methyl-4-oxo-1-naphthoyl)thiomorpholine

124. 3-(piperidinomethyl)-4-(1,2,3,4-tetrahydro-6-methyl-1-naphthoyl)thiomorpholine

125. 4-(3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)morpholine

126. 4-(5-chloro-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)morpholine

127. 4-(5,6-dichloro-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)morpholine

128. 3-(pyrrolidin-1-ylmethyl)-4-(1,2,3,4-tetrahydro-4-oxo-1-naphthoyl)morpholine

129. 3-(pyrrolidin-1-ylmethyl)-4-(1,2,3,4-tetrahydro-1-naphthoyl)morpholine

130. 4-(6,7-dichloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl)-3-(pyrrolidin-1-ylmethyl)morpholine

131. 4-(6,7-dichloro-1,2,3,4-tetrahydro-1-naphthoyl)-3-(pyrrolidin-1-ylmethyl)morpholine

132. 4-(5-chloro-3-oxoindan-1-carbonyl)-3-(dimethylaminomethyl)morpholine

133. 4-methyl-1-(3-oxoindan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperazine

134. 1-(indan-1-carbonyl)-4-methyl-2-(pyrrolidin-1-ylmethyl)piperazine

135. 3-(pyrrolidin-1-ylmethyl)-4-(1,2,3,4-tetrahydro-4-oxo-1-naphthoyl)thiomorpholine

136. 3-(pyrrolidin-1-ylmethyl)-4-(1,2,3,4-tetrahydro-1-naphthoyl)thiomorpholine

137. 4-(6-chloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

138. 4-(6-chloro-1,2,3,4-tetrahydro-1-naphthoyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

139. 3-(pyrrolidin-1-ylmethyl)-4-(1,2,3,4-tetrahydro-6-methyl-4-oxo-1-naphthoyl)thiomorpholine

140. 3-(pyrrolidin-1-ylmethyl)-4-(1,2,3,4-tetrahydro-6-methyl-1-naphthoyl)thiomorpholine

141. 3-(pyrrolidin-1-ylmethyl)-4-(1,2,3,4-tetrahydro-6-isopropyl-4-oxo-1-naphthoyl)thiomorpholine

142. 3-(pyrrolidin-1-ylmethyl)-4-(1,2,3,4-tetrahydro-6-isopropyl-1-naphthoyl)thiomorpholine

143. 4-(5,6-difluoroindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

144. 4-(5,6-difluoro-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

145. 4-(5,6-dimethylindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

146. 4-(5,6-dimethyl-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

147. 4-(6-methylindan-1-carbonyl)-3-(piperidinomethyl)thiomorpholine

148. 4-(6-methyl-3-oxoindan-1-carbonyl)-3-(piperidinomethyl)thiomorpholine

149. 4-(6-isopropylindan-1-carbonyl)-3-(piperidinomethyl)thiomorpholine

150. 4-(6-isopropyl-3-oxoindan-1-carbonyl)-3-(piperidinomethyl)thiomorpholine

151. 4-(5,6-dichloroindan-1-carbonyl)-3-(piperidinomethyl)thiomorpholine

152. 4-(5,6-dimethylindan-1-carbonyl)-3-(piperidinomethyl)thiomorpholine

153. 4-(5,6-dimethyl-3-oxoindan-1-carbonyl)-3-(piperidinomethyl)thiomorpholine

154. 4-(5,6-difluoroindan-1-carbonyl)-3-(piperidinomethyl)thiomorpholine

155. 4-(5,6-difluoro-3-oxoindan-1-carbonyl)-3-(piperidinomethyl)thiomorpholine

156. 4-(5,6-dichloro-3-oxoindan-1-carbonyl)-3-(piperidinomethyl)thiomorpholine

157. 1-(5-chloro-3-oxoindan-1-carbonyl)-4-methyl-2-(pyrrolidin-1-ylmethyl)piperazine

158. 1-(5-chloroindan-1-carbonyl)-4-methyl-2-(pyrrolidin-1-ylmethyl)piperazine

159. 4-(5-chloroindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)morpholine

160. 4-methyl-2-(pyrrolidin-1-ylmethyl)-1-(1,2,3,4-tetrahydro-4-oxo-1-naphthoyl)piperazine

161. 4-methyl-2-(pyrrolidin-1-ylmethyl)-1-(1,2,3,4-tetrahydro-1-naphthoyl)piperazine

162. 1-(5,6-dichloro-3-oxoindan-1-carbonyl)-4-methyl-2-(pyrrolidin-1-ylmethyl)piperazine

163. 1-(5,6-dichloroindan-1-carbonyl)-4-methyl-2-(pyrrolidin-1-ylmethyl)piperazine

164. 1-(6-chloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl)-4-methyl-2-(pyrrolidin-1-ylmethyl)piperazine

165. 1-(1,2,3,4-tetrahydro-6-chloro-1-naphthoyl)-4-methyl-2-(pyrrolidin-1-ylmethyl)piperazine

166. 1-(5-methyl-3-oxoindan-1-carbonyl)-4-methyl-2-(pyrrolidin-1-ylmethyl)piperazine

167. 4-(5-methyl-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)piperazine

168. 1-(6,7-dichloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl)-4-methyl-2-(pyrrolidin-1-ylmethyl)piperazine

169. 1-(6,7-dichloro-1,2,3,4-tetrahydro-1-naphthoyl)-4-methyl-2-(pyrrolidin-1-ylmethyl)piperazine

170. 4-(5,6-dichloro-3-oxoindan-1-carbonyl)-3-(morpholinomethyl)morpholine

171. 4-(6,7-dichloro.-4-oxo-1,2,3,4-tetrahydro-1-naphthoyl)-3-(piperidinomethyl)thiomorpholine

172. 1-(5-methylthio-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

173. 1-(5,6-dichloroindan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine

174. 1-(5,6-dichloro-3-oxoindan-1-carbonyl)-2-(morpholinomethyl)piperidine

175. 4-[2-(3,4-dichlorophenyl)propionyl]-3-(pyrrolidin-1-ylmethyl)thiomorpholine

176. 4-(5-trifluoromethyl-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

Preferred compounds within this list include Compound Numbers 1, 2, 4, 9, 10, 13, 14, 16, 17, 19, 20 23, 24, 25, 26, 28. 30, 32, 36, 38, 42, 44, 49, 50, 51, 55, 56, 57, 60, 63, 64, 65, 68, 69, 70, 71, 72, 73, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 91, 95, 96, 97, 98, 99, 102, 104, 105, 110, 111, 112, 113, 118, 119, 120, 121, 123, 125, 126, 127, 130, 131, 132, 135, 136, 137, 138, 139, 140, 143, 144, 147, 148, 151, 154, 155, 156, 160, 162, 164, 168, 170, 171, 172, 173 and 175 and their salts, especially their hydrochlorides, and their isomeric forms.

More preferred compounds within this list include Compound Numbers 9, 10, 13, 14, 17, 23, 30, 32, 49, 63, 72, 73, 79, 80, 102, 105, 110, 113, 118, 123, 127, 130, 137, 139, 144, 147, 148, 151, 156, 162, and 171, and their salts, especially their hydrochlorides, and their isomeric forms.

Most preferred compounds within this list include Compound Numbers 9, 13, 30, 72, 73, 79, 80, 113, 118, 151, 156, and 171, and their salts, especially their hydrochlorides, and their isomeric forms.

The novel carboxylic acid amide derivatives of this invention, including the acid addition salts, exhibit useful pharmacological effects, such as anti-inflammatory and analgesic activity.

The pharmacological activity of compounds of this invention was examined according to recognised procedures.

p-Phenylquinone-induced writhing in mice

Testing was performed essentially according to the procedure of Siegmund et al. reported in Proceedings of Society for Experimental Biology & Medicine 95, 729 (1957).

Male ddY mice (Japan SLC) each weighing about 20 g were divided into groups each including from 5 to 10 mice, and were fasted for 16 hours from the day before the test. A compound to be tested was dissolved in physiological saline, and injected subcutaneously. After 15 minutes, 0.1 ml/mouse of 0.03% p-phenylquinone was injected intraperitoneally. Five minutes later, the frequency of writhing reactions in the mouse was counted for the following 10 minutes. For the control mice, only physiological saline solution was injected. Mice in which the frequency of writhing reactions was decreased to a half or less of the mean frequency of writhing reactions in the control mice were regarded as analgesic-effective mice. The ratio, analgesic-effective animals/all animals, was obtained for every dosage, and then ED₅₀ values (50% effective dose) were calculated according to the probit method. For some test compounds the test was modified to determine the writhing effect at a dose of 320 μg/kg.

Affinity to receptors

A raw preparation from brain membrane was made according to the method of Pasuternak et al. [Molecular Pharmacology 11, 340 (1975)]. The whole brains were taken from male Hartley guinea pigs each weighing from 400 to 700 g (Japan SLC) and the cerebella were removed. One part of the whole brain sample was homogenized in 30 parts of ice-cooled 50 mM Tris buffer solution (pH 7.4) by use of a Polytron homogenizer, and then, centrifuged for 15 minutes at 49,000×g. The precipitated pellet was suspended in the same kind of buffer. The suspension was incubated for 30 minutes at 37° C., and centrifuged for 15 minutes at 49,000×g. One part of the precipitate was suspended in 30 parts of the buffer solution, and preserved at -80° C. Before use, the suspension was melted, homogenized using a Dounce-type homogenizer, and diluted to a final protein concentration of 0.5 mg/ml.

Binding to κ-receptors was tested essentially according to the method reported in Archives of Pharmacology 319, 197 (1982) by Magnan et al. Taking 0.6 nM of tritium-labelled ethylketocyclazocine as a labelled ligand, binding to the brain membranous preparation was examined by addition of 100 nM of DAGO (D-Ala², MePhe⁴, Gly-ol⁵ enkephalin) and 10 nM of DADLE ([D-Ala², D-Leu⁵ ]-enkephalin) to saturate the μ- and δ-receptors. The membranous preparation, labelled ligand, cold ligand and compound to be tested were incubated in 1 ml of Tris buffer at 25° C. for 45 minutes. Then, the mixture was mixed with 5 ml of ice-cooled buffer solution, filtered through Watmann GF/B filter paper under reduced pressure, and washed twice. The filter paper was placed in an emulsion scintillation (ACS-II) and allowed to stand overnight, and then the radioactivity was measured by a liquid scintillation counter. The affinity of test compound to the receptor was assessed as the concentration required to inhibit binding of the labelled ligand by 50% (IC₅₀, nM).

Binding to μ-receptors was tested according to the procedure of Magnan et al. mentioned above. By using 1 nM of tritium-labelled DAGO as a labelled ligand, the test was carried out in a similar manner to that mentioned in the experiment for testing binding to κ-receptors. The affinity of test compound was assessed as an IC₅₀.

The results of the tests are summarized in the following Table, and indicate that compounds of general formula (I), and acid addition salts, are useful as analgesic agents.

                  TABLE                                                            ______________________________________                                                   Analgesic effect                                                               Phenylquinone-      Binding to                                                 induced writhing    opioid receptors                                 Example   ED.sub.50           (IC.sub.50, nM)                                  compound  μg/kg s.c.                                                                           320 μg/kg                                                                              κ                                                                              μ                                       ______________________________________                                         1         6.20                1.75  1068                                       2-E.sub.1 1.73                0.90  232                                        4-D.sub.1 3.43                1.40  531                                        2-E.sub.2 320                 258   10000                                      4-D.sub.2 270                 366   10000                                      17                 5/5        1.1   --                                         36        3.4                 2.4   1135                                       41-D.sub.1                                                                               1.3                 0.67  698.2                                      U-50488E  490      2/5        9.92  636                                        Morphine HCl                                                                             480      2/5        552   5.1                                        ______________________________________                                          Compound U50488E is                                                            trans3,4-dichloro-N-methyl-N-[2(1-pyrrolidinyl)cyclohexyl]benzeneacetamid     , see J. Pharmacol. Exp. Ther. (1983) 224, 7                              

For the administration route of the compounds of this invention, there may be mentioned injection; the oral route using tablets, capsules, granules, powders or syrups; the perintestinal route using suppositories; or the parenteral route using ointments, creams or patches. Though variable depending on the symptoms, age, body weight and other factors, the usual daily dose for an adult person for the typical administration routes is 0.005 mg to 10 mg given by injection, 0.01 to 10 mg given by patches, or 0.1 mg to 100 mg given by oral route. The daily dosage may be given once or divided into several doses.

The novel compounds of the present invention of general formula (I) can be synthesized by conventional processes such as those employed for amide synthesis, using starting materials which are known or which may be prepared by analogy with the preparation of known compounds.

Typically, an acid of general formula (II); ##STR6## (wherein R³, R⁴, and ring A are as defined) is reacted optionally in the form of a derivative with an amine of general formula (III): ##STR7## (wherein R¹, R² and E are as defined).

For example, the acid of the general formula (II) may be employed in the reaction with the amine of the general formula (III) in the form of a derivative which is an acyl halide such as acyl chloride, acyl bromide, of acyl iodide. Such a reaction can be carried out in the presence of a base in an inert solvent. Preferred bases include an organic amine such as triethylamine or DBU; or an inorganic base such as sodium carbonate, potassium carbonate, sodium hydroxide or potassium hydroxide. As appropriate depending mainly on the choice of base, the solvent can be an organic solvent or an aqueous solvent. Preferred organic solvents include a halogenated hydrocarbon such as methylene chloride, chloroform, carbon tetrachloride or 1,2-dichloroethane; or an ether such as diethyl ether, tetrahydrofuran or 1,4-dioxane. Preferred aqueous solvents include water or aqueous organic solvents. For this reaction in the case of using an organic or inorganic base in an organic solvent, the temperature is usually from -30° C. to the reflux temperature of the solvent, more typically from -10° C. to room temperature. On the other hand, for this reaction in the case of using an organic or inorganic base in an aqueous solvent, the temperature is usually from -5° to 0° C. Though variable depending on the reaction temperature and the like, the reaction usually takes from 30 minutes to 3 hours.

In another example of synthesis of the present compounds, the acid of the general formula (II) may be employed in the reaction with the amine of the general formula (III) in the form of a derivative which is a mixed acid anhydride. Such an anhydride can readily be obtained by reacting the acid for instance with a haloformate of general formula Hal-COOR⁵ (where R⁵ represents a C₁ -C₃ alkyl group such as a methyl or ethyl group, and Hal represents a halogen atom such as a chlorine or bromine atom), in the presence of organic base in an inert solvent to give a mixed acid anhydride. For the solvent; a halogenated hydrocarbon such as methylene chloride, 1,2-dichloroethane, carbon tetrachloride or chloroform, an amide such as dimethylformamide, or an ether such as diethyl ether, tetrahydrofuran or 1,4-dioxane is preferred. For the organic base, a tertiary amine such as triethylamine, N-methylmorpholine or an organic amine such as pyridine is preferred. The reaction is preferably carried out at from -20° C. to the reflux temperature of the solvent employed, and usually requires from 30 minutes to 12 hours. The resulting acid anhydride can then be allowed to react with an amine compound of the general formula (III). Usually this reaction is carried out without isolation of the anhydride from the solvent containing organic base, but more generally the reaction is carried out using conditions similar to those mentioned above for the reaction of an acyl chloride with the amine (III).

In a further example of amide formation, the reaction using a condensing reagent; for example, the Mukaiyama reaction can be employed. This reaction is generally performed in the presence of a condensing reagent such as triphenylphosphine and 2,2'-pyridine disulfide (for a Mukaiyama reaction), or 1,3-dicyclohexylcarbodiimide (DCC), in an inert solvent. The solvent is typically a polar solvent such as an ether, for example tetrahydrofuran, a nitrile, for example acetonitrile, or an amide, for example dimethylformamide. The reaction is normally carried out at from -20° C. to 100° C. Though variable depending on the reaction temperature, the reaction usually requires 30 minutes to 24 hours.

Variations in the process employed for production of the compounds of general formula (I) can be adopted. For instance, the acid of the general formula (II) may be employed in the reaction with the amine of the general formula (III) in the form of a derivative which is an appropriately unsaturated acid. Such an unsaturated acid may be reacted with the amine to form an unsaturated amide, which is then reduced to give a compound of formula (I). This method can be generally employed to produce compounds of formula (I) where R³ and R⁴ represent the group of formula (IV) and thus form a ring fused to ring A. In this instance, the starting acid can have a double bond in the ring fused to the ring A, which double bond may be reduced in conventional manner after amide formation. In particular, for the preparation of 3-oxoindan-1-carbonyl amides, the starting acid may be a 3-oxo-1-indene-1-carboxylic acid which is reacted optionally as a reactive derivative with an amine of general formula (III) and then reduced to convert the indene ring to an indan ring.

After completion of the amide formation, the desired compound of the general formula (I) can be obtained from the reaction mixture by conventional means. The compound can be purified, for example, by chromatography or by preparing an acid addition salt such as a hydrochloride.

In general, the compounds of the general formula (I) can, if desired, be converted into a pharmaceutically acceptable acid addition salt by treatment with an inorganic acid such as hydrochloric acid, hydrobromic acid, hydroiodic acid, sulfuric acid or phosphoric acid, or with an organic acid such as oxalic acid, fumaric acid, maleic acid, mandelic acid, citric acid, tartaric acid, benzenesulfonic acid, p-toluenesulfonic acid, methanesulfonic acid or ethanesulfonic acid.

The compounds of the general formula (I) exist as diastereoisomers and optical isomers, due to the presence of asymmetric carbon atoms in the molecule. If desired, one or more of the isomers of compound (I) can be separated from a mixture of the isomers by a conventional isolation method, or the optical isomers of compound (I) can be obtained by amide formation using an optically resolved starting material of general formula (II) and/or (III).

EXAMPLES OF THE INVENTION

The present invention is illustrated by the following non-limiting Examples, which include a Pharmaceutical Example and a Preparative Example. Some compounds prepared in the Examples are diastereoisomers for which the absolute configuration is not known. For such compounds, prefixes R* or S* are employed, indicating the compound in question is a racemic mixture. Thus, (1S*, 2S*) means a 1:1 mixture of (1R, 2R) and (1S, 2S) and is the same as (1R*, 2R*). Correspondingly, (1R*, 2R*) means a 1:1 mixture of (1R, 2S) and (1S, 2R) and is the same as (1S*, 2R*).

Example 1

1-(5,6-dichloro-3-oxoindin-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine hydrochloride

3.5 g (21.4 m mol) of 2-(pyrrolidin-1-ylmethyl)piperidine dihydrochloride (synthesized according to the method of U.S. Pat. No. 2,684,965) was added to 85.6 ml (85.6 m mol) of 1N sodium hydroxide solution cooled at from 0° C. to -5° C. The mixture was stirred for 30 minutes, then 20 ml of methylene chloride containing 5.63 g of 5,6-dichloro-3-oxoindan-1-carbonyl chloride (prepared by conventional synthesis from its corresponding acid made according to the procedure reported by Lahiri et al. in J. Indian Chem. Soc. 53, 1041 (1976)) was added dropwise to the mixture. The mixture was stirred for 90 minutes at -5° C., and then for 3 hours at room temperature.

After completion of the reaction, the reaction mixture was poured into ice water and extracted with diethyl ether. The extract was washed with saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was distilled off and, the residue was subjected to column chromatography to obtain 1.31 g of the desired compound by elution with a mixed solvent of ethyl acetate, triethylamine and ethanol (100:1:1). The product was dissolved in acetone, mixed with a 4N 1,4-dioxane solution of hydrogen chloride, evaporated down, and recrystallized from a mixed solvent of ethanol, acetone and diethyl ether (1:1:2), to give 1.24 g of the title compound melting at 239°-242° C. (dec).

Elemental analysis (%) C₂₀ H₂₅ Cl₃ N₂ O₂ Calcd C, 55.63; H, 5.84; N, 6.49; Cl, 24.63 Found C, 55.11; H, 5.64; N, 6.39; Cl, 24.14.

Example 2

1-(5,6-dichloro-3-oxoindan-1-carbonyl)-(2S)-2-(pyrrolidin-1-ylmethyl)piperidine hydrochloride

15 ml of methylene chloride solution containing 3.13 g (11.88 m mol) of 5,6-dichloro-3-oxoindan-1-carbonyl chloride was added dropwise at -10° C. to 15 ml of methylene chloride solution containing 1 g (5.94 m mol) of (2S)-2-(pyrrolidin-1-ylmethyl)piperidine and 1.82 ml (13.07 m mol) of triethylamine. After the addition, the reaction mixture was stirred at -10° C. for 1 hour, poured into ice water and extracted with methylene chloride. The methylene chloride extract was washed with saturated aqueous sodium chloride solution and dried over anhydrous sodium sulfate. After evaporation of the solvent, a mixture of two optically active isomers was obtained. Medium pressure liquid chromatography of the mixture using a mixed solvent of ethyl acetate and triethylamine (100:1) gave 0.65 g (27.7%) of one of the optically active isomers, E₁, eluted earlier, and 1.0 g (42.6%) of the other optically active isomer, E₂, eluted later.

Isomer E₁ was dissolved in acetone and mixed with a 4N 1,4-dioxane solution of hydrogen chloride. After evaporation down, the residue was recrystallized from a mixed solvent of methanol, acetone and diethyl ether to afford colorless prisms melting at 243°-244° C. (dec), and showing [α]_(D) +36° (c=0.5, methanol).

In a similar way, Isomer E₂ in the form of the hydrochloride was obtained as colorless needles melting at 194°-196° C. (dec), and showing [α]_(D) -56° (c=0.5, methanol).

Isomer E₁ is 1-[(1S)-5,6-dichloro-3-oxoindan-1-carbonyl]-(2S)-2-(pyrrolidin-1-ylmethyl)piperidine, and isomer E₂ is 1-[(1R)-5,6-dichloro-3-oxoindan-1-carbonyl]-(2S)-2-(pyrrolidin-1-ylmethyl)piperidine.

Isomer E₁ hydrochloride

Elemental analysis (%) C₂₀ H₂₅ Cl₃ N₂ O₂ Calcd C, 55.63; H, 5.84; N, 6.49; Cl, 24.63 Found C, 55.77; H, 5.88; N, 6.49; Cl, 24.65

Isomer E₂ hydrochloride

Elemental analysis (%) C₂₀ H₂₅ Cl₃ N₂ O₂ Calcd C, 55.63; H, 5.84; N, 6.49; Cl, 24.63 Found C, 55.31; H, 5.87; N, 6.48; Cl, 22.38.

Example 3

1-(5,6-dichloro-3-oxoindan-1-carbonyl)-(2R)-2-(pyrrolidin-1-ylmethyl)piperidine hydrochloride

By following a procedure similar to that in Example 2, two optical isomers were obtained as their hydrochlorides from 1.25 g of (2R)-2-(pyrrolidin-1-ylmethyl)piperidine. 1.5 g of triethylamine and 1.96 g of 5,6-dichloro-3-oxoindan-1-carbonyl chloride. The products comprised 0.45 g of the hydrochloride of one of the optically active isomers (E₁), melting at 248°-250° C. (dec), and showing [α]_(D) -37° (c=0.5, methanol), and 0.38 g of the hydrochloride of the other isomer (E₂), melting at 199°-201° C. (dec), and showing [α]_(D) +58° (c=0.5, methanol).

Isomer E₁ is 1-[(1R)-5,6-dichloro-3-oxoindan-1-carbonyl]-(2R)-2-(pyrrolidin-1-ylmethyl)piperidine, and isomer E₂ is 1-[(1S)-5,6-dichloro-3-oxoindan-1-carbonyl]-(2R)-2-(pyrrolidin-1-ylmethyl)piperidine.

Isomer E₁ hydrochloride

Elemental analysis (%) C₂₀ H₂₅ Cl₃ N₂ O₂ Calcd C. 55.63; H, 5.84; N, 6.49; Cl, 24.63 Found C, 55.60; H, 5.78; N, 6.31; Cl, 24.49

Isomer E₂ hydrochloride

Elemental analysis (%) C₂₀ H₂₅ Cl₃ N₂ O₂ Calcd C, 55.63; H, 5.84; N, 6.49; Cl, 24.63 Found C, 55.33; H, 5.90; N, 6.38; Cl, 24.55.

Example 4

1-[(1S*)-5,6-dichloro-3-oxoindan-1-carbonyl]-(2S*)-2-(pyrrolidin-1-ylmethyl)piperidine hydrochloride and 1-[(1R*)-5,6-dichloro-3-oxoindan-1-carbonyl]-(2S*)-2-(pyrrolidin-1-ylmethyl)piperidine hydrochloride

Using a procedure similar to that in Example 1, the title compounds were obtained from 5.0 g of 2-(pyrrolidin-1-ylmethyl)piperidine dihydrochloride, 5.3 g of 5,6-dichloro-3-oxoindan-1-carbonyl chloride and 80 ml of 1N aqueous sodium hydroxide solution. By medium pressure liquid chromatographic separation using a mixed solvent of ethyl acetate and triethylamine (100:1), 0.85 g of one of the diastereoisomers, D₁, eluted earlier, and 0.88 g of the other diastereoisomer, D₂, eluted later, were obtained. When each of these isomers was converted into its corresponding hydrochloride by treatment with a 4N 1,4-dioxane solution of hydrogen chloride, 0.97 g of the hydrochloride of isomer D₁, melting at 253°-255° C. (dec) and 0.83 g of the hydrochloride of the other isomer, D₂, melting at 228°-230° C. (dec) were obtained.

Diastereoisomer D₁ is 1-[(1S*)-5,6-dichloro-3-oxoindan-1-carbonyl]-(2S*)-2-(pyrrolidin-1-ylmethyl)piperidine and diastereoisomer D₂ is 1-[(1R*)-5,6-dichloro-3-oxoindan-1-carbonyl]-(2S*)-2-(pyrrolidin-1-ylmethyl)piperidine

Diastereoisomer D₁ hydrochloride

Elemental analysis (%) C₂₀ H₂₅ Cl₃ N₂ O₂ Calcd C, 55.63; H, 5.84; N, 6.49; Cl, 24.63 Found C, 55.48; H, 5.85; N, 6.47; Cl, 24.82

Diastereoisomer D₂ hydrochloride

Elemental analysis (%) C₂₀ H₂₅ Cl₃ N₂ O₂ Calcd C, 55.63; H, 5.84; N, 6.49; Cl, 24.63 Found C, 53.90; H, 6.00; N, 6.12; Cl, 24.83.

Example 5

1-(3-oxoindan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine hydrochloride

From 1.74 g of 2-(pyrrolidin-1-ylmethyl)piperidine, 2.21 g of 3-oxoindan-1-carbonyl chloride and 2.16 ml of triethylamine, 1.21 g of the title compound was obtained, melting at 190°-215° C. (dec), using a procedure similar to that in Example 2.

Elemental analysis (%) C₂₀ H₂₇ ClN₂ O₂ Calcd C, 66.19; H, 7.50; N, 7.72; Cl, 9.77 Found C, 66.00; H, 7.62; N, 7.56; Cl, 9.56.

Example 6

1-(5-methyl-3-oxoindan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine hydrochloride

From 2.7 g of 2-(pyrrolidin-1-ylmethyl)piperidine, 3.0 g of 5-methyl-3-oxoindan-1-carbonyl chloride and 2.0 g of triethylamine, 2.1 g of the title compound was obtained, melting at 153°-154° C. using a procedure similar to that in Example 2.

Elemental analysis (%) C₂₁ H₂₉ ClN₂ O₂ Calcd C, 66.92; H, 7.76; N, 7.43; Cl, 9.41 Found C, 66.69; H, 7.80; N, 7.29; Cl, 9.23.

Example 7

1-(5-chloro-3-oxoindan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine hydrochloride

To 100 ml of tetrahydrofuran solution containing 2.1 g of 5-chloro-3-oxoindan-1-carboxylic acid and 1.5 ml of triethylamine, 1.1 ml of ethyl chloroformate was added dropwise at -20° C. The reaction mixture was stirred for 20 minutes, 1.7 g of 2-(pyrrolidin-1-ylmethyl)piperidine was added, and the mixture was stirred for an additional 30 minutes. The reaction mixture was stirred further for 1 hour at room temperature. After completion of the reaction, the reaction mixture was poured into ice water and extracted with diethyl ether. The extract was washed with water, dried over anhydrous sodium sulfate, and the solvent was distilled off. The residue was subjected to silica gel column chromatography to obtain 0.8 g of the free amine of the title compound by elution with a mixed solvent of ethyl acetate and triethylamine (50:1). By treatment with a 4N 1,4-dioxane solution of hydrogen chloride, 0.6 g of the title compound was obtained, melting at 225°-230° C.

Elemental analysis (%) C₂₀ H₂₆ Cl₂ N₂ O₂ Calcd C, 60.46; H, 6.60; N, 7.05; Cl, 17.84 Found C, 60.19; H, 6.80; N, 6.99; Cl, 17.64.

Example 8

1-(6-methoxy-3-oxoindan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine hydrochloride

From 1.21 g of 2-(pyrrolidin-1-ylmethyl)piperidine dihydrochloride, 1.35 g of 6-methoxy-3-oxoindan-1-carbonyl chloride and 2.79 ml of triethylamine, 0.72 g of the title compound was obtained, melting at 210°-228° C. (dec) using a procedure similar to that in Example 2.

Elemental analysis (%) C₂₁ H₂₉ ClN₂ O₃ ·1/2 H₂ O Calcd C, 62.75; H, 7.52; N, 6.97; Cl, 8.82 Found C, 62.51; H, 7.45; N, 6.83; Cl, 9.27.

Example 9

1-(4,5-dichloro-3-oxoindan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine hydrochloride

From 1.18 g of 2-(pyrrolidin-1-ylmethyl)piperidine, 2.03 g of 4,5-dichloro-3-oxoindan-1-carbonyl chloride and 1.47 ml of triethylamine, 0.95 g of the title compound was obtained, melting at 148°-150° C. (dec) using a procedure similar to that in Example 2.

Elemental analysis (%) C₂₀ H₂₅ Cl₃ N₂ O₂ Calcd C, 55.63; H, 5.84; N, 6.49; Cl, 24.63 Found C, 55.11; H, 5.64; N, 6.39; Cl, 24.14.

Example 10

1-(6-hydroxy-3-oxoindan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine hydrochloride

From 1.21 g of 2-(pyrrolidin-1-ylmethyl)piperidine dihydrochloride, 1.26 g of 6-hydroxy-3-oxoindan-1-carbonyl chloride and 2.8 ml of triethylamine, 0.1 g of the title compound was obtained, melting at 220°-231° C. (dec), using a procedure similar to that in Example 2.

Elemental analysis (%) C₂₀ H₂₇ ClN₂ O₃ Calcd C, 63.40; H, 7.18; N, 7.39; Cl, 9.36 Found C, 63.60; H, 7.22; N, 7.84; Cl, 10.36.

Example 11

1-(5,6-dichloro-3-oxoindan-1-carbonyl)-2-(piperidinomethyl)piperidine hydrochloride.

From 1.5 g of 2-(piperidinomethyl)piperidine dihydrochloride, 2.5 g of 5,6-dichloro-3-oxoindan-1-carbonyl chloride and 45 ml of 1N aqueous sodium hydroxide solution, 1.1 g of the title compound was obtained, melting at 240°-245° C. (dec), using a procedure similar to that in Example 1.

Elemental analysis (%) C₂₁ H₂₇ Cl₃ N₂ O₃ Calcd C, 54.62; H, 5.89; N, 6.07; Cl, 23.03 Found C, 54.60; H, 5.99; N, 6.00; Cl, 22.96.

Example 12

1-(1,2,3,4-tetrahydro-4-oxo-1-naphthoyl)-2-(pyrrolidin-1-ylmethyl)piperidine hydrochloride

From 3.48 g of 2-(pyrrolidin-1-ylmethyl)piperidine dihydrochloride, 4.44 g of 1,2,3,4-tetrahydro-4-oxo-1-naphthoyl chloride and 63.9 ml of 1N aqueous sodium hydroxide solution, 4.17 g of the title compound was obtained, melting at 239°-242° C. (dec), using a procedure similar to that in Example 1.

Elemental analysis (%) C₂₁ H₂₉ ClN₂ O₂ Calcd C, 66.92; H, 7.76; N, 7.43; Cl, 9.41 Found C, 66.34; H, 7.72; N, 7.24; Cl, 9.06.

Example 13

1-(6,7-dichloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl)-2-(pyrrolidin-1-yl-methyl)piperidine hydrochloride

From 0.89 g of 2-(pyrrolidin-1-ylmethyl)piperidine, 1.61 g of 6,7-dichloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl chloride and 11 ml of triethylamine, 1.5 g of the title compound was obtained, melting at 255°-257° C. (dec), using a procedure similar to that in Example 2.

Elemental analysis C₂₁ H₂₇ Cl₃ N₂ O₂ Calcd C, 56.58; H, 6.10; N, 6.28; Cl, 23.86 Found C, 55.86; H, 6.13; N, 6.16; Cl, 23.48.

Example 14

4,5-dihydro-6-oxo-4-[2-(pyrrolidin-1-ylmethyl)piperidine-1-carbonyl]-6H-cyclopenta[b]thiophene hydrochloride

From 1.68 g of 2-(pyrrolidin-1-ylmethyl)piperidine, 2.2 g of 4,5-dihydro-6-oxo-6H-cyclopenta[b]thiophene-4-carbonyl chloride and 2.09 ml of triethylamine, 1.02 g of the title compound was obtained, melting at 189°-218° C. (dec), using a procedure similar to that in Example 2.

Elemental analysis (%) C₁₈ H₂₅ ClN₂ O₂ S·1/2 H₂ O Calcd C, 57.20; H, 6.68; N, 7.41; Cl, 9.38; S, 8.48 Found C, 56.91; H, 6.87; N, 7.13; Cl, 9.09; S, 8.25.

Example 15

1-(5-nitro-3-oxoindan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine hydrochloride

From 1.21 g of 2-(pyrrolidin-1-ylmethyl)piperidine dihydrochloride, 1.32 g of 5-nitro-3-oxoindan-1-carbonyl chloride and 2.8 ml of triethylamine, 0.05 g of the title compound was obtained, melting at 154°-160° C. (dec), using a procedure similar to that in Example 2.

Elemental analysis (%) C₂₀ H₂₆ ClN₃ O₄ Calcd C, 58.89; H, 6.43; N, 10.30; Cl, 8.69 Found C, 58.59; H, 6.29; N, 10.17; Cl, 8.48.

Example 16

1-(indan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine hydrochloride

From 2.36 g of 2-(pyrrolidin-1-ylmethyl)piperidine, 2.5 g of indene-1-carbonyl chloride and 4.88 ml of triethylamine, 1.4 g of 1-(indene-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine was obtained using a procedure similar to that in Example 2. In a mixed solvent of methanol, water and ethanol (2:1:1), this compound was catalytically reduced with 10% palladium on carbon. After completion of the reduction, the catalyst was filtered off. After evaporation of the solvent, the residue was treated with a 4N 1,4-dioxane solution of hydrogen chloride to obtain 1.05 g of the title compound, melting at 218°-221° C.

Elemental analysis (%) C₂₀ H₂₇ ClN₂ O Calcd C, 69.25; H, 7.85; N, 8.08; Cl, 10.22 Found C, 69.26; H, 8.01; N, 7.60; Cl, 10.89.

Example 17

4-(3,4-dichlorophenylacetyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine hydrochloride

3-(Pyrrolidin-1-ylmethyl)thiomorpholine was generated from the corresponding hydrochloride, prepared as described in the Preparative Example which follows the Examples. A solution of 1.49 ml of triethylamine, and 1.0 g of 3-(pyrrolidin-1-ylmethyl)thiomorpholine dissolved in 50 ml of methylene chloride was cooled to 0° C. in an atmosphere of nitrogen with vigorous stirring. To the solution was added dropwise 5 ml of methylene chloride containing 1.44 g of 3,4-dichlorophenylacetyl chloride and the mixture was stirred at 3° C. for an hour and subsequently for 4 hours at room temperature.

After completion of the reaction, the reaction mixture was poured into a solution of sodium bicarbonate and extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate followed by concentration of the solvent by distillation under reduced pressure. The residue was purified by column chromatography through silica gel and 1.39 g of the desired compound was obtained from the fractions eluted with a 3:1 mixture of ethyl acetate and methanol. The product was dissolved in 20 ml of methylene chloride and mixed with a molar equivalent of a 4N 1,4-dioxane solution of hydrogen chloride. The mixture was concentrated and the residue was recrystallized from a mixture of ethanol and acetone to afford the title compound as colorless crystals, melting at 230°-239° C. (dec.).

Elemental analysis (%) C₁₇ H₂₃ Cl₃ N₂ OS Calcd C, 49.83; H, 5.66; Cl, 25.95; N, 6.84; S, 7.82 Found C, 49.69; H, 5.69; Cl, 25.52; N, 6.53; S, 7.55.

Example 18

4-(3,4-dichlorophenylacetyl)-3-(pyrrolidin-1-ylmethyl)morpholine hydrochloride

The procedure described in Example 17 was repeated, but using 1.64 g of 3-(pyrrolidin-1-ylmethyl)morpholine, 3.72 ml of triethylamine and 1.54 g of 3,4-dichlorophenylacetyl chloride, to afford 0.72 g of the title compound, melting at 268° (dec.).

Elemental analysis (%) C₁₇ H₂₃ Cl₃ N₂ O₂ Calcd C, 51.86; H, 5.89; N, 7.11; Cl, 27.01 Found C, 51.68; H, 5.97; N, 7.20; Cl, 26.73.

Example 19

1-(3,4-dichlorophenylacetyl)-4-methyl-2-(pyrrolidin-1-ylmethyl)piperazine dihydrochloride

The procedure described in Example 17, but using 1.0 g of 1-methyl-3-(pyrrolidin-1-ylmethyl)piperazine trihydrochloride. 2.1 ml of triethylamine and 0.8 g of 3,4-dichlorophenylacetyl chloride, to afford 1.01 g of the title compound, melting at 223°-227° C. (dec.).

Elemental analysis (%) C₁₈ H₂₇ Cl₄ N₃ O·1/2 H₂ O Calcd C, 47.80; H, 6.24; N, 9.29; Cl, 31.36 Found C, 47.63; H, 6.06; N, 9.40; Cl, 31.40.

Example 20

4-(4-methylphenylacetyl)-3-(pyrrolidin-1-ylmethyl)morpholine hydrochloride

To a solution of 1.33 g of 3-(pyrrolidin-1-ylmethyl)morpholine dihydrochloride in 30 ml of methylene chloride was added 1.5 ml of an aqueous solution containing 0.66 g of sodium hydroxide at 5° C. After the mixture was stirred vigorously, the organic layer was separated and dried over anhydrous magnesium sulfate. To a solution of 0.8 g of 4-methylphenylacetic acid, 0.78 ml of triethylamine and one drop of N-methylmorpholine in 30 ml of tetrahydrofuran was added a tetrahydrofuran solution containing 0.55 ml of ethyl chloroformate, followed by stirring at -20° to -15° C. for 20 minutes. To this stirred mixture was then added the previously prepared methylene chloride solution of 3-(pyrrolidin-1-ylmethyl)morpholine. The mixture was stirred at the same temperature for 30 minutes and subsequently for an hour at room temperature. After completion of the reaction, the reaction mixture was washed with a saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate.. After distilling off the solvent, the residue was purified by column chromatography through silica gel and 0.56 g of the desired produced was obtained from the fraction eluted with a 3:1 mixture of ethyl acetate and methanol. The product was dissolved in methylene chloride and mixed with a molar equivalent of a 4N 1,4-dioxane solution of hydrogen chloride. The mixture was concentrated and recrystallized from a mixture of methanol and diethyl ether to afford the title compound, melting at 131° (dec.).

Elemental analysis (%) C₁₈ H₂₇ ClN₂ O₂ ·H₂ O Calcd C, 60.58; H, 8.19; N, 7.85; Cl, 9.93 Found C, 61.16; H, 8.04; N, 7.78; Cl, 9.99.

Example 21

4-(4-methylthiophenylacetyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine hydrochloride

The procedure described in Example 17 was repeated, but using 1.0 g of 3-(pyrrolidin-1-ylmethyl)thiomorpholine, 1.38 ml of triethylamine and 1.2 of 4-methylthiophenylacetyl chloride, to afford 1.38 g of the title compound, melting at 162°-166° C. (dec.).

Elemental analysis (%) C₁₈ H₂₆ ClN₂ OS₂ Calcd C, 55.86; H, 7.03; N, 7.24; Cl, 9.16; S, 16.57 Found C, 55.48; H, 6.95; N, 6.96; Cl, 8.92; S, 16.83.

Example 22

3-(pyrrolidin-1-ylmethyl)-4-(2-thienylacetyl)thiomorpholine hydrochloride

The procedure described in Example 17 was repeated, but using 1.0 g of 3-(pyrrolidin-1-ylmethyl)thiomorpholine, 2.49 ml of triethylamine and 1.03 g of 2-thienylacetyl chloride, to afford 0.37 g of the title compound, melting at 204°-206° C. (dec.).

Elemental analysis (%) C₁₅ H₂₃ ClN₂ OS₂ Calcd C, 51.93; H, 6,68; N, 8.07; Cl, 10.22; S, 18.48 Found C, 51.85; H, 6.66; N, 8.10; Cl, 10.43; S, 18.24.

Example 23

3-(pyrrolidin-1-ylmethyl)-4-(2-thienylacetyl)morpholine hydrochloride

The procedure described in Example 17 was repeated, but using 0.88 g of 3-(pyrrolidin-1-ylmethyl)morpholine, 2.0 ml of triethylamine and 0.45 g of 2-thienylacetyl chloride, to afford 0.71 g of the title compound, melting at 215° C. (dec.).

Elemental analysis (%) C₁₅ H₂₃ ClN₂ O₂ S Calcd C, 54.45; H, 7,01; N, 8.47; Cl, 10.71; S, 9.69 Found C, 54.44; H, 7.08; N, 8.58; Cl, 10.72; S, 9.61.

Example 24

1-(5,6-dichloro-3-oxoindan-1-carbonyl)-4-methyl-2-(pyrrolidin-1-ylmethyl)piperazine dihydrochloride

To a suspension of 2.0 g of 4-methyl-2-(pyrrolidin-1-ylmethyl)piperazine trihydrochloride in 150 ml of methylene chloride was added 4.3 ml of triethylamine with vigorous stirring in an atmosphere of nitrogen. After stirring for 20 minutes, the mixture was cooled to -10° C. in an ice and salt bath and 50 ml of methylene chloride solution containing 1.9 g of 5,6-dichloro-3-oxoindan-1-carbonyl chloride was added dropwise to it. The reaction mixture was stirred at -10° C. for an hour and a half and subsequently at room temperature for two hours and a half and poured into a saturated aqueous solution of sodium bicarbonate. The resulting aqueous mixture was extracted with diethyl ether and the extract was washed with a saturated aqueous solution of sodium chloride followed by drying over anhydrous magnesium sulfate and distilling off the solvent. The residue was purified by column chromatography through silica gel and 1.60 g of the desired compound was obtained from the fractions eluted with a 10:3 mixture of ethyl acetate and triethylamine. To a solution of the product dissolved in methylene chloride was added a two molar quantity of a 4N 1,4-dioxane solution of hydrogen chloride and the mixture was concentrated. The residue was recrystallized from a mixture of ethanol and acetone to afford the title compound, melting at 250°-255° C. (dec.).

Elemental analysis (%) C₂₀ H₂₇ Cl₄ N₃ O₂ ·1/2 H₂ O Calcd C, 48.80; H, 5.73; N, 8.54; Cl, 28.81 Found C, 49.20; H, 5.73; N, 8.54; Cl, 29.05.

Example 25

4-methyl-1-(5-methyl-3-oxoindan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperazine dihydrochloride

The procedure described in Example 24 was repeated, but using 1.0 g of 1-methyl-3-(pyrrolidin-1-ylmethyl)piperazine trihydrochloride, 2.1 ml of triethylamine and 0.75 g of 5-methyl-3-oxoindan-1-carbonyl chloride, to afford 0.84 g of the title compound, melting at 220°-223° C. (dec.).

Elemental analysis (%) C₂₁ H₃₁ Cl₂ N₃ O₂ ·1/2 H₂ O Calcd C, 57.66; H, 7.37; N, 9.61; Cl, 16.21 Found C, 57.86; H, 7.42; N, 9.32; Cl, 16.07.

Example 26

4-methyl-1-(3-oxoindan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperazine dihydrochloride

The procedure described in Example 24 was repeated, but using 3.21 g of 1-methyl-3-(pyrrolidin-1-ylmethyl)piperidine trihydrochloride, 6.9 ml of triethylamine and 4.5 g of 3-oxoindan-1-carbonyl chloride, to afford 1.45 g of the title compound, melting at 252°-255° C. (dec.).

Elemental analysis (%) C₂₀ H₂₉ Cl₂ N₃ O₂ ·1/2 H₂ O Calcd C, 56.74; H, 7.14; N, 9.92; Cl, 16.75 Found C, 56.57; H, 7.25; N, 9.69; Cl, 16.56.

Example 27

1-(5,6-dichloroindan-1-carbonyl)-4-methyl-2-(pyrrolidin-1-ylmethyl)piperazine dihydrochloride

The procedure described in Example 24 was repeated, but using 1.67 g of 1-methyl-3-(pyrrolidin-1-ylmethyl)piperazine trihydrochloride, 3.6 ml of triethylamine and 1.5 g of 5,6-dichloroindan-1-carbonyl chloride, to afford 1.54 g of the title compound, melting at 245°-250° C.

Elemental analysis (%) C₂₀ H₂₉ Cl₄ N₃ O·1/2 H₂ O Calcd C, 50.23; H, 6.32; N, 8.79; Cl, 29.65 Found C, 50.09; H, 6.23; N, 8.74; Cl, 29.56.

Example 28

1-(6,7-dichloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl)-4-methyl-2-(pyrrolidin-1-ylmethyl)piperazine dihydrochloride

The procedure described in Example 24 was repeated, but using 1.0 g of 1-methyl-3-(pyrrolidin-1-ylmethyl)piperazine trihydrochloride, 2.1 ml of triethylamine and 1.0 g of 6,7-dichloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl chloride, to afford 0.97 g of the title compound, melting at 275°-278° C. (dec.).

Elemental analysis (%) C₂₁ H₂₉ Cl₄ N₃ O₂ ·1/2 H₂ O Calcd C, 49.82; H, 5.97; N, 8.30; Cl, 28.01 Found C, 50.12; H, 5.83; N, 8.32; Cl, 27.90.

Example 29

1-(6-chloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl)-4-methyl-2-(pyrrolidin-1-ylmethyl)piperazine dihydrochloride

The procedure described in Example 24 was repeated, but using 1.0 g of 1-methyl-3-(pyrrolidin-1-ylmethyl)piperazine trihydrochloride, 2.1 ml of triethylamine and 0.87 g of 6-chloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl chloride, to afford 0.92 g of the title compound, melting at 268°-274° C. (dec.).

Elemental analysis (%) C₂₁ H₃₀ Cl₃ N₃ O₂ Calcd C, 54.50; H, 6.53; N, 9.08; Cl, 22.98 Found C, 54.68; H, 6.36; N, 9.01; Cl, 22.64.

Example 30

4-(5,6-dichloro-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)morpholine hydrochloride

The procedure described in Example 24 was repeated, but using 0.88 g of 3-(pyrrolidin-1-ylmethyl)morpholine, 2.0 ml of triethylamine and 1.0 g of 5,6-dichloro-3-oxo-indan-1-carbonyl chloride, to afford 0.66 g of the title compound, melting at 250°-257° C. (dec.).

Elemental analysis (%) C₁₉ H₂₃ Cl₃ N₂ O₃ ·H₂ O Calcd C, 50.51; H, 5.58; N, 6.20; Cl, 23.50 Found C, 50.43; H, 5.58; N, 6.27; Cl, 23.72.

Example 31

4-(3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)morpholine hydrochloride

The procedure described in Example 24 was repeated, but using 0.86 g of 3-(pyrrolidin-1-ylmethyl)morpholine, 1.96 ml of triethylamine and 0.89 g of 3-oxoindan-1-carbonyl chloride, to afford 0.35 g of the title compound, melting at 260°-265° C. (dec.).

Elemental analysis C₁₉ H₂₅ ClN₂ O₃ Calcd C, 62.54; H, 6.91; N, 7.68; Cl, 9.72 Found C, 62.26; H, 7.02; N, 7.73; Cl, 9.75.

Example 32

4-(5-methyl-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)morpholine hydrochloride

The procedure described in Example 24 was repeated, but using 0.89 g of 3-(pyrrolidin-1-ylmethyl)morpholine, 2.2 ml of triethylamine and 0.83 g of 5-methyl-3-oxoindan-1-carbonyl chloride, to afford 0.23 g of the title compound, melting at 225°-230° C.

Elemental analysis (%) C₂₀ H₂₇ ClN₂ O₃ Calcd C, 63.40; H, 7.18; N, 7.39; Cl, 9.36 Found C, 63.50; H, 7.09; N, 7.40; Cl, 9.49.

Example 33

4-(5-chloro-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)morpholine hydrochloride

The procedure described in Example 24 was repeated, but using 0.89 g of 3-(pyrrolidin-1-ylmethyl)morpholine, 2.0 ml of triethylamine and 0.91 g of 5-chloro-3-oxoindan-1-carbonyl chloride, to afford 0.83 g of the title compound, melting at 220°-229° C. (dec.).

Elemental analysis (%) C₁₉ H₂₄ Cl₂ N₂ O₃ Calcd C, 57.15; H, 6.06; N, 7.02; Cl, 17.76 Found C, 56.90; H, 6.01; N, 7.00; Cl, 17.55.

Example 34

4-(5,6-dichloro-3-oxoindan-1-carbonyl)-3-(morpholinomethyl)morpholine hydrochloride

The procedure described in Example 24 was repeated, but using 1.25 g of 3-(morpholinomethyl)morpholine, 2.67 ml of triethylamine and 1.11 g of 5,6-dichloro-3-oxoindan-1-carbonyl chloride, to afford 0.7 g of the title compound, melting at 210°-216° C. (dec.).

Elemental analysis (%) C₁₉ H₂₃ Cl₃ N₂ O₄ Calcd C, 50.74; H, 5.15; N, 6.23; Cl, 23.65 Found C, 50.43; H, 5.04; N, 6.16; Cl, 23.40.

Example 35

4-(5-chloro-3-oxoindan-1-carbonyl)-3-(dimethylaminomethyl)morpholine hydrochloride

The procedure described in Example 24 was repeated, but using 0.90 g of 3-dimethylaminomethylmorpholine, 2.3 ml of triethylamine and 1.03 g of 5-chloro-3-oxoindan-1-carbonyl chloride, to afford 1.03 g of the title compound, melting at 230°-240° C.

Elemental analysis (%) C₁₇ H₂₂ Cl₂ N₂ O₃ Calcd C, 54.70; H, 5.94; N, 7.50; Cl, 19.00 Found C, 54.36; H, 6.28; N, 7.28; Cl, 19.21.

Example 36

4-(5,6-dichloro-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine hydrochloride

The procedure described in Example 24 was repeated, but using 0.6 g of 3-(pyrrolidin-1-ylmethyl)thiomorpholine, 0.6 g of triethylamine and 1.0 g of 5,6-dichloro-3-oxoindan-1-carbonyl chloride, to afford 0.39 g of the title compound, melting at 215°-223° C.

Elemental analysis (%) C₁₉ H₂₃ Cl₃ N₂ O₂ S·H₂ O Calcd C, 48.74; H, 5.34; N, 5.99; S, 6.85 Found C, 48.46; H, 5.34; N, 5.90; S, 7.02.

Example 37

4-(5-methyl-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine hydrochloride

The procedure described in Example 24 was repeated, but using 0.92 g of 3-(pyrrolidin-1-ylmethyl)thiomorpholine, 1.64 ml of triethylamine and 1.66 g of 5-methyl-3-oxoindan-1-carbonyl chloride, to afford 1.35 g of the title compound, melting at 232°-234° C.

Elemental analysis (%) C₂₀ H₂₇ ClN₂ O₂ S Calcd C, 60.82; H, 6.89; N, 7.09; Cl, 8.97; S, 8.11 Found C, 60.57; H, 6.77; N, 7.06; Cl, 8.69; S, 8.38

Example 38

4-(5-chloro-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine.multidot.hydrochloride

The procedure described in Example 24 was repeated, but using 3.7 g of 3-(pyrrolidin-1-ylmethyl)thiomorpholine, 3.42 ml of triethylamine and 4.56 g of 5-chloro-3-oxoindan-1-carbonyl chloride, to afford 2.8 g of the title compound, melting at 200°-205° C. (dec.).

Elemental analysis (%) C₁₉ H₂₄ Cl₂ N₂ O₂ S Calcd C, 54.94; H, 5.82; N, 6.74; Cl, 17.07; S, 7.72 Found C, 54.99; H, 6.02; N, 6.65; Cl, 16.82; S, 7.63.

Example 39

4-(6-methoxy-3-oxoindan-1-carbonyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine hydrochloride

The procedure described in Example 24 was repeated, but using 0.97 g of 3-(pyrrolidin-1-ylmethyl)thiomorpholine, 1.39 ml of triethylamine and 1.23 g of 6-methoxy-3-oxoindan-1-carbonyl chloride, to afford 0.9 g of the title compound, melting at 225°-233° C.

Elemental analysis (%) C₂₀ H₂₇ ClN₂ O₃ S Calcd C, 58.45; H, 6.62; N, 6.82; Cl, 8.63; S, 7.80 Found C, 58.55; H, 6.85; N, 6.59; Cl, 8.50; S, 7.62.

Example 40

4,5-dihydro-6-oxo-4-[3-(pyrrolidin-1-ylmethyl)thiomorpholine-1-carbonyl]-6H-cyclopenta[b]thiophene hydrochloride

The procedure described in Example 24 was repeated, but using 0.96 g of 3-(pyrrolidin-1-ylmethyl)thiomorpholine, 1.39 ml of triethylamine and 1.0 g of 4,5-dihydro-6-oxo-6H-cyclopenta[b]thiophene-4-carbonyl chloride, to afford 0.5 g of the title compound, melting at 204°-223° C.

Elemental analysis (%) C₁₇ H₂₃ ClN₂ O₂ S₂ ·1/2 H₂ O Calcd C, 51.57; H, 6.11; N, 7.07; Cl, 8.95; S, 16.19 Found C, 51.71; H, 6.09; N, 7.08; Cl, 8.76; S, 16.30.

Example 41

4-[(1S*)-5,6-dichloroindan-1-carbonyl]-(3S*)-3-(pyrrolidin-1-ylmethyl)thiomorpholine hydrochloride, and

4-[(1R*)-5,6-dichloroindan-1-carbonyl]-(3S*)-3-(pyrrolidin-1-ylmethyl)thiomorpholine hydrochloride

The procedure described in Example 24 was repeated, but using 0.72 g of 3-(pyrrolidin-1-ylmethyl)thiomorpholine, 0.8 ml of triethylamine and 1.08 g of 5,6-dichloroindan-1-carbonyl chloride, to afford the title compounds as diastereoisomers, which were separated by column chromatography under medium pressure using a mixed solvent of ethyl acetate and triethylamine (100:1). There were obtained 0.57 g of diastereoisomer D₁ in the earlier effluent and 0.19 g of diastereotsomer D₂ in the later effluent. Each diastereotsomer was converted to diastereoisomer D₁ hydrochloride, melting at 220°-230° C. and diastereoisomer D₂ hydrochloride, melting at 230°-242° C., respectively.

Diastereoisomer D₁ is 4-[(1S*)-5,6-dichloroindan-1-carbonyl]-(3S*)-3-(pyrrolidin-1-ylmethyl)thiomorpholine, and diastereoisomer D₂ is 4-[(1R*)-5,6-dichloroindan-1-carbonyl]-(3S*)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

Diastereoisomer D₁ hydrochloride

Elemental analysis (%) C₁₉ H₂₅ Cl₃ N₂ OS Calcd C, 52.36; H, 5.78; N, 6.43; Cl, 24.40; S, 7.36 Found C, 52.25; H, 5.70; N, 6.50; Cl, 24.61; S, 7.35

Diastereotsomer D₂ hydrochloride

Elemental analysis (%) C₁₉ H₂₅ Cl₃ N₂ OS Calcd C, 52.36; H, 5.78; N, 6.43; Cl, 24.40; S, 7.36 Found C, 52.28; H, 5.70; N, 6.60; Cl, 24.52; S, 7.29.

Example 42

4-(5,6-dichloro-3-oxoindan-1-carbonyl)-3-(piperidinomethyl)thiomorpholine hydrochloride

The procedure described in Example 24 was repeated, but using 0.9 g of 3-(piperidinomethyl)thiomorpholine, 1.0 g of triethylamine and 1.5 g of 5,6-dichloro-3-oxoindan-1-carbonyl chloride, to afford 0.45 g of the title compound, melting at 146°-155° C.

Elemental analysis (%) C₂₀ H₂₅ Cl₃ N₂ O₂ S·H₂ O Calcd C, 49.80; H, 5.60; N, 5.81; Cl, 22.07; S, 6.65 Found C, 49.54; H, 5.57; N, 5.81; Cl, 22.35; S, 6.70.

Example 43

4-[(1S*)-6,7-dichloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl]-(3S*)-3-(pyrrolidin-1-ylmethyl)thiomorpholine hydrochloride, and

4-[(1R*)-6,7-dichloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl]-(3S*)-3-(pyrrolidin-1-ylmethyl)thiomorpholine hydrochloride

According to a manner similar to that of Example 24, the reaction products prepared from 3.7 g of 3-(pyrrolidin-1-ylmethyl)thiomorpholine, 3.4 ml of triethylamine and 5.5 g of 6,7-dichloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl chloride were separated by column chromatography under medium pressure using a mixed solvent of ethyl acetate and triethylamine (100:1). Diastereoisomer D₁ (1.9 g) was obtained from the fractions eluted earlier and diastereoisomer D₂ (2.8 g) from the fractions eluted later. Each isomer was converted into diastereoisomer D₁ hydrochloride, melting at 263°-264° C. and diastereoisomer D₂ hydrochloride, melting at 264°-265° C., respectively.

Diastereoisomer D₁ is 4-[(1S*)-6,7-dichloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl]-(3S,)-3-(pyrrolidinylmethyl)thiomorpholine hydrochloride, and diastereoisomer D₂ is 4-[(1R*)-6,7-dichloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl]-(3S*)-3-(pyrrolidin-1-ylmethyl)thiomorpholine hydrochloride

Diastereotsomer D₁ hydrochloride

Elemental analysis (%) C₂₀ H₂₅ N₂ O₂ Cl₃ S Calcd C, 51.79; H, 5.43; N, 6.04; Cl, 22.93; S, 6.91 Found C, 51.57; H, 5.70; N, 5.90; Cl, 23.02; S, 6.85

Diastereoisomer D₂ hydrochloride

Elemental analysis (%) C₂₀ H₂₅ N₂ O₂ Cl₃ S Calcd C, 51.79; H, 5.43; N, 6.04; Cl, 22.93; S, 6.91 Found C, 51.79; H, 5.69; N, 6.05; Cl, 22.86; S, 6.86.

Example 44

4-(6-chloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl)-3-(pyrrolidin-1-ylmethyl)thiomorpholine hydrochloride

The procedure described in Example 24 was repeated, but using 1.0 g of 3-(pyrrolidin-1-ylmethyl)thiomorpholine, 1.38 ml of triethylamine and 1.5 g of 6-chloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl chloride, to afford 1.76 g of the title compound, melting at 195°-200° C.

Elemental analysis (%) C₂₀ H₂₆ N₂ O₂ C₁₂ S·H₂ O Calcd C, 53.69; H, 6.30; N, 6.26; Cl, 15.85; S, 7.17 Found C, 53.72; H, 6.04; N, 6.28; Cl, 15.58; S, 7.07.

Example 45

4-(6,7-dichloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl)-3-(piperidinomethyl)thiomorpholine hydrochloride

The procedure described in Example 24 was repeated, but using 2.0 g of 3-(piperidinomethyl)thiomorpholine, 2.2 ml of triethylamine and 3.52 g of 6,7-dichloro-1,2,3,4-tetrahydro-4-oxo-1-naphthoyl chloride, to afford 3.67 g of the title compound, melting at 245°-254° C. (dec.).

Elemental analysis (%) C₂₁ H₂₇ N₂ O₂ Cl₃ S Calcd C, 52.78; H, 5.70;. N, 5.86; Cl, 22.26; S, 6.71 Found C, 53.00; H, 6.01; N, 5.60; Cl, 21.93; S, 6.47.

Example 46

4-(5,6-dichloro-3-oxoindan-1-carbonyl)-(3R)-3-(pyrrolidin-1-ylmethyl)thiomorpholine

A solution (15 ml) of 3.0 g of 5,6-dichloro-3-oxoindan-1-carboxylic acid chloride in methylene chloride was dropwise added at -10° C. to a 15 ml of methylene chloride solution of (3R)-3-(pyrrolidin-1-ylmethyl)thiomorpholine (1 g) and triethylamine (2 ml). The reaction mixture was stirred for 1 hour at -10° C. and poured into ice-water. The mixture was extracted with methylene chloride. Then, the extract was washed with a saturated solution of sodium chloride and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give a mixture of two optical isomers. This mixture was subjected to medium pressure liquid chromatography and eluted using a mixed solvent of ethyl acetate and triethylamine (100:1), to yield 0.8 g of an optical isomer E₁ (oil) as a first fraction and 1.0 g of an optical isomer E₂ (oil) as a second fraction. Isomer E₁ is the (1S) isomer, and isomer E₂ is the (1R) isomer.

Example 47

1-(5,6-dichloroindan-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine hydrochloride

From 1.18 g of 2-(pyrrolidin-1-ylmethyl)piperidine, and 1.87 g of 5,6-dichloroindan-1-carbonyl chloride, 0.51 g of the title compound was obtained, melting at 245°-250° C., using a procedure similar to that in Example 1.

Elemental analysis (%) C₂₀ H₂₇ Cl₃ N₂ O Calcd C, 57.50; H, 6.51; N, 6.70; Cl, 25.46 Found C, 57.25; H, 6.58; N, 6.62; Cl, 25.25.

Example 48

1-(5,6-dichloro-3-oxoindan-1-carbonyl)-2-(morpholinomethyl)piperidine hydrochloride

From 0.93 g of 2-(morpholinomethyl)piperidine, and 1.00 g of 5,6-dichloro-3-oxoindan-1-carbonyl chloride, 0.85 g of the title compound was obtained, melting at 235°-240° C., using a procedure similar to that in Example 1.

Elemental analysis (%) C₂₀ H₂₅ Cl₃ N₂ O₃ Calcd C, 53.65; H, 5.63; N, 6.26; Cl, 23.75 Found C, 53.47; H, 5.72; N, 6.31; Cl, 23.57.

Example 49

4-[2-(3,4-dichlorophenyl)propionyl]-3-(pyrrolidin-1-ylmethyl)thiomorpholine hydrochloride

From 1.86 g of 3-(pyrrolidin-1-ylmethyl)thiomorpholine, and 2.4 g of 2-(3,4-dichlorophenyl)propionyl chloride, 0.71 g of the title compound was obtained, melting at 224°-230° C., using a procedure similar to that in Example 1.

Elemental analysis (%) C₁₈ H₂₅ Cl₃ N₂ OS Calcd C, 51.00; H, 5.90; N, 6.61; Cl, 25.15; S, 7.56 Found C, 51.18; H, 6.05; N, 6.60; Cl, 25.57; S, 7.22.

Pharmaceutical Example

Capsule

The compound of Example 36 (1 mg) was triturated in to a 1:50 compound with lactose, and the resulting powder was again triturated in to a 1:20 powder with lactose, giving Powder A.

100 mg of Powder A and 0.5 mg of magnesium stearate were packed in to capsules (No. 5).

Preparative Example

3-(pyrrolidin-1-ylmethyl)thiomorpholine dihydrochloride

(a) 4-(t-butoxycarbonyl)thiomorpholine-3-carboxylic acid

Triethylamine (23.6 ml) was added at 0° C. to a solution of DL-thiomorpholine-3-carboxylic acid (5 g) in 40 ml of a 1:1 mixture of 1,4-dioxane and water. Thereafter, di-t-butyl dicarbonate (8.16 g) was added and the reaction mixture was stirred for 30 minutes at 0° C. and for 3 hours at room temperature. The solvent was evaporated under reduced pressure and the residue was dissolved in 100 ml of ethyl acetate. The pH of the reaction solution was adjusted to 4 using saturated citric acid solution and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was recrystallized from hexane/ethyl acetate to yield 6.0 g (71%) of 4-(t-butoxycarbonyl)thiomorpholine-3-carboxylic acid.

(b) 3-(Pyrrolidine-1-carbonyl)thiomorpholine

Triethylamine (3.1 ml), followed by a solution of pyrrolidine (2.0 ml) in 10 ml of tetrahydrofuran, was added at 0° C. under a stream of nitrogen to a solution of 5.0 g of 4-(t-butoxycarbonyl)thiomorpholine-3-carboxylic acid in 100 ml of tetrahydrofuran. After the mixture had been stirred for 1 hour, a solution of 3.6 g of ethyl cyanophosphate in 10 ml of tetrahydrofuran was added to the mixture and the mixture was stirred for 5 hours. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and the solvent was concentrated under reduced pressure. The residue was recrystallized from ethyl acetate/hexane to yield 4.61 g (74%) of 4-(t-butoxycarbonyl)-3-(pyrrolidine-1-carbonyl)thiomorpholine.

4-(t-butoxycarbonyl)-3-(pyrrolidine-1-carbonyl)thiomorpholine (3.2 g) was dissolved in 50 ml of methanol. A 4N 1,4-dioxane solution of hydrogen chloride (13.1 ml) was added, and the solution was condensed to yield white crystals. These crystals was recrystallized from ethanol and diethyl ether to give 2.47 g (96%) of 3-(pyrrolidine-1-carbonyl)thiomorpholine monohydrochloride.

A 1N aqueous sodium hydroxide solution (12.5 ml) was added to a mixture of 2.47 g of 3-(pyrrolidine-1-carbonyl)thiomorpholine monohydrochloride and 20 ml of methylene chloride. The organic layer was extracted and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to yield 1.75 g (83%) of 3-(pyrrolidine-1-carbonyl)thiomorpholine

(c) 3-(pyrrolidin-1-ylmethyl)thiomorpholine dihydrochloride

A solution of 1.6 g of 3-(pyrrolidine-1-carbonyl)thiomorpholine in 200 ml of tetrahydrofuran was added dropwise to a mixture of 1.0 g of lithium alminum hydride and 100 ml of tetrahydrofuran under ice-cooling and a stream of nitrogen. Excess lithium alminum hydride was decomposed using 15 g of sodium sulfate decahydrate. Celite filtration using methylene chloride was carried out. The solvent was concentrated under reduced pressure to yield 1.37 g (93%) of 3-(pyrrolidin-1-ylmethyl)thiomorpholine.

A mixture of 260 mg of 3-(pyrrolidin-1-ylmethyl)thiomorpholine and 5 ml of 1,4-dioxane was treated with 150 μl of 4N 1,4-dioxane solution of hydrogen chloride. The solvent was evaporated under reduced pressure to yield 354 mg (98%) of 3-(pyrrolidin-1-ylmethyl)thiomorpholine dihydrochloride, melting at 218°-220° C.

Elemental Analysis (%) C₉ H₂₀ N₂ SCl₂ Calcd C, 41.70; H, 7.78; N, 10.80; S, 12.37; Cl, 27.35 Found C, 41.57; H, 8.04; N, 10.61; S, 12.25; Cl, 27.30. 

We claim:
 1. A process for preparing a compound of the formula (I): ##STR8## in which, R¹ and R² are the same or different and each is selected from the group consisting of a hydrogen atom and C₁ -C₆ alkyl groups, or R¹ and R² together with the nitrogen atom to which they are attached form a heterocyclic ring which is unsubstituted or substituted and is a 5-membered or a 6-membered N-heterocycle which optionally has a further heteroatom selected from the group consisting of oxygen, nitrogen and sulfur;E is selected from the group consisting of a sulfur atom, an unsubstituted imino group, and imino groups substituted with a substituent selected from the group consisting of C₁ -C₆ alkyl groups and aralkyl groups; ring A is selected from the group consisting of unsubstituted aryl rings; unsubstituted heteroaryl rings; aryl rings substituted with at least one substituent of a Group (i); and heteroaryl rings substituted with at least one substituent said Group (i); said Group (i) represents halogen atoms, C₁ -C₆ alkyl groups, halogenated C₁ -C₆ alkyl groups, C₁ -C₆ alkoxy groups, halogenated C₁ -C₆ alkoxy groups, C₁ -C₆ alkylthio groups, aryl groups, acyl groups, nitro groups, and hydroxy groups; R³ represents a hydrogen atom or a C₁ -C₆ alkyl group and R⁴ represents a hydrogen atom, or R³ and R⁴ together represent a group of formula (IV)

    --(CR.sup.a R.sup.b).sub.m --C(═Y)--                   (IV)

wherein each R^(a) and R^(b) represents hydrogen or a C₁ -C₃ alkyl group, provided that there are not more than three alkyl groups in the group of formula (IV), m represents 1, 2, or 3, and Y represents two hydrogen atoms or an oxygen atom; or a pharmaceutically acceptable salt thereof; which process comprises reacting an acid of formula (II) ##STR9## wherein R³ R⁴, and ring A are as defined above, with an amine of formula (III) ##STR10## wherein R¹, R² and E are as defined above.
 2. The process of claim 1, wherein the acid of the formula (II) is employed in the form of a derivative which is an acyl halide or a mixed acid anhydride, or the acid of formula (II) is reacted with the amine of formula (III) in the presence of condensing reagent, or the acid of the formula (II) is employed in the form of a derivative which is an unsaturated acid which is reduced after the reaction with the amine of formula (III).
 3. The process of claim 1, wherein the compound of formula (I) is converted into a pharmaceutically acceptable acid addition salt.
 4. The process of claim 1, wherein the acid of formula (II) is in the form of a derivative.
 5. The process of claim 4, wherein the derivative is an acyl halide.
 6. The process of claim 5, wherein the acyl halide is selected from the group consisting of acyl chloride, acyl bromide and acyl iodide.
 7. The process of claim 1, which further comprises carrying out the process in the presence of a base in an inert solvent.
 8. The process of claim 7, wherein the base is selected from the group consisting of triethylamine, sodium carbonate, potassium carbonate, sodium hydroxide and potassium hydroxide.
 9. The process of claim 8, wherein the solvent is an organic solvent selected from the group consisting of methylene chloride, chloroform, carbon tetrachloride, 1,2-dichloroethane, diethyl ether, tetrahydrofuran and 1,4-dioxane.
 10. The process of claim 9, wherein the process is carried out at a temperature of -30° C. to the reflux temperature of the solvent.
 11. The process of claim 10, wherein the temperature is -10° C. to room temperature.
 12. The process of claim 8, wherein the solvent is water and the process is carried out at a temperature of -5° C. to 0° C.
 13. The process of claim 11, which further comprises carrying out the process for 30 minutes to 3 hours.
 14. The process of claim 12, which further comprises carrying out the process for 30 minutes to 3 hours.
 15. The process of claim 2, wherein the acid of the formula (II) is in a form of a mixed acid anhydride which is obtained by reacting the acid with a haloformate of the formula Hal--COOR⁵, wherein R⁵ is a C₁ -C₃ alkyl, in the presence of an organic base in an inert solvent, at a temperature of -20° C. to the reflux temperature of the solvent for 30 minutes to 12 hours.
 16. The process of claim 2, wherein the acid of the formula (II) is reacted with the amine of the formula (III) in the presence of a condensing agent selected from the group consisting of triphenylphosphine, 2,2'-pyridine disulfide and 1,3-dicyclohexylcarbodiimide, in a solvent selected from the group consisting of tetrahydrofuran, acetonitrile and dimethylformamide, at a temperature of -20° C. to 100° C. and for 30 minutes to 24 hours.
 17. The process of claim 1, wherein when E is NH, and one or both of R¹ and R² are not hydrogen.
 18. The process of claim 2, wherein R¹ and R² together with the nitrogen atom to which they are attached form a heterocyclic ring which is selected from the group consisting of imidazolidinyl, hexahydropyridazinyl, hexahydropyrimidinyl, piperazinyl, hexamethyleneimino, 1,2-diazacycloheptyl, 1,3-diazacycloheptyl, homopiperazinyl, pyrrolyl, azepinyl, thiazolidinyl, morpholinyl, thiomorpholinyl, pyrazolyl, imidazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, 1,2,3-oxadiazolyl, triazolyl, tetrazolyl, thiadiazolyl, pyridyl, pyridazinyl, pyrimidinyl, pyrazinyl, quinolyl, isoquinolyl, acridyl, tetrahydroacridyl, pyrrolidinyl, piperidino, tetrahydroquinolyl, tetrahydroisoquinolyl, isoindolyl, indolinyl and 6-azabicyclo(3.2.1)oct-6-yl, said heterocyclic ring being unsubstituted or substituted by a straight or branched C₁ -C₆ alkyl group. 